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Literature SNPs List
Total result: 1391
rs_ID
|
Location
|
Functional Annotation
|
No. of Studies (significant/non-significant/trend) 
|
|---|---|---|---|
| rs1800955 | chr11:636784(Fwd) | upstream_gene_variant | 3 (2/1/0) |
| rs4570308 | chrX:43511497(Fwd) | upstream_gene_variant | 1 (1/0/0) |
| rs1728818 | chr3:11032992(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs1331504 | chr9:93405828(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs2112347 | chr5:75015242(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs4448731 | chr12:72329106(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs2652510 | chr5:1447860(Fwd) | upstream_gene_variant | 2 (0/2/0) |
| rs7848810 | chr9:93407858(Fwd) | upstream_gene_variant | 1 (1/0/0) |
| rs2652511 | chr5:1446389(Fwd) | upstream_gene_variant | 6 (4/1/1) |
| rs521674 | chr10:112835590(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs7160641 | chr14:97056727(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs13268919 | chr8:23096594(Fwd) | upstream_gene_variant | 1 (0/0/1) |
| rs130056 | chr6:78173631(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs2693727 | chr7:129417730(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs1412005 | chr9:93409161(Fwd) | upstream_gene_variant | 1 (1/0/0) |
| rs9860697 | chr3:165557079(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs6064361 | chr20:54841008(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs3758653 | chr11:636399(Fwd) | upstream_gene_variant | 2 (1/1/0) |
| rs5953210 | chrX:43514046(Fwd) | upstream_gene_variant | 1 (1/0/0) |
| rs8047014 | chr16:69135049(Fwd) | upstream_gene_variant | 1 (0/0/1) |
| rs6919857 | chr6:137140454(Fwd) | upstream_gene_variant | 2 (0/2/0) |
| rs267418 | chr5:174880645(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs1503433 | chr3:88037200(Fwd) | upstream_gene_variant | 1 (1/0/0) |
| rs4795541 | chr17:28564360(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs28362317 | chr5:1447844(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs12720373 | chr11:636688(Fwd) | upstream_gene_variant | 1 (1/0/0) |
| rs7149784 | chr14:97057998(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs10485813 | chr20:51583983(Fwd) | upstream_gene_variant | 1 (0/0/1) |
| rs1800544 | chr10:112836503(Fwd) | upstream_gene_variant | 12 (1/11/0) |
| rs11564750 | chr5:1447762(Fwd) | upstream_gene_variant | 6 (3/3/0) |
| rs1980818 | chr20:54840706(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs2550956 | chr5:1447841(Fwd) | upstream_gene_variant | 2 (0/2/0) |
| rs6311 | chr13:47471478(Fwd) | upstream_gene_variant | 5 (1/4/0) |
| rs4783899 | chr16:55687212(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs1611115 | chr9:136500515(Fwd) | upstream_gene_variant | 7 (2/5/0) |
| rs936461 | chr11:636496(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs916457 | chr11:637014(Fwd) | upstream_gene_variant | 1 (1/0/0) |
| rs2617595 | chr5:1448246(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs1076150 | chr9:136498761(Fwd) | upstream_gene_variant | 1 (1/0/0) |
| rs7036351 | chr9:34592699(Fwd) | upstream_gene_variant | 1 (1/0/0) |
| rs2731886 | chr5:36606009(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs11178997 | chr12:72332153(Fwd) | upstream_gene_variant | 1 (1/0/0) |
| rs2397771 | chr16:55689087(Fwd) | upstream_gene_variant | 2 (0/2/0) |
| rs2361209 | chr3:143568783(Fwd) | upstream_gene_variant | 1 (1/0/0) |
| rs3813929 | chrX:113818520(Fwd) | upstream_gene_variant | 2 (1/1/0) |
| rs10492555 | chr13:36709109(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs4570625 | chr12:72331923(Fwd) | upstream_gene_variant | 4 (1/3/0) |
| rs2617596 | chr5:1446719(Fwd) | upstream_gene_variant | 1 (1/0/0) |
| rs7645681 | chr3:143568154(Fwd) | upstream_gene_variant | 1 (1/0/0) |
| rs6582071 | chr12:72330112(Fwd) | upstream_gene_variant | 1 (1/0/0) |
| rs2975226 | chr5:1445616(Fwd) | upstream_gene_variant | 2 (2/0/0) |
| rs676643 | chr1:23521340(Fwd) | upstream_gene_variant | 1 (1/0/0) |
| rs916455 | chr11:636929(Fwd) | upstream_gene_variant | 2 (0/2/0) |
| rs689687 | chr9:93410201(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs2652509 | chr5:1448247(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs2550946 | chr5:1450513(Fwd) | upstream_gene_variant | 3 (2/1/0) |
| rs17053121 | chr4:168157594(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs7963717 | chr12:72331362(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs7682295 | chr4:3765225(Fwd) | upstream_gene_variant | 1 (1/0/0) |
| rs1362621 | chr16:55688484(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs623580 | chr11:18063977(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs7105122 | chr11:47449544(Fwd) | upstream_gene_variant | 1 (0/0/1) |
| rs10064219 | chr5:1384998(Fwd) | upstream_gene_variant | 1 (0/1/0) |
| rs28386840 | chr16:55686818(Fwd) | upstream_gene_variant | 2 (0/2/0) |
| rs2550948 | chr5:1450444(Fwd) | upstream_gene_variant | 2 (2/0/0) |
| rs11079828 | chr17:46609103(Fwd) | upstream_gene_variant | 1 (0/0/1) |
| rs3756450 | chr5:1448148(Fwd) | upstream_gene_variant | 1 (1/0/0) |
| rs9850088 | chr3:143567690(Fwd) | upstream_gene_variant | 1 (1/0/0) |
| rs34586911 | chr4:62453069(Fwd) | synonymous_variant; upstream_gene_variant | 1 (0/0/1) |
| rs6350 | chr5:1443199(Fwd) | synonymous_variant; upstream_gene_variant | 2 (1/1/0) |
| rs28364998 | chr5:1403112(Fwd) | synonymous_variant; upstream_gene_variant | 1 (0/0/1) |
| rs2291560 | chr7:128477472(Fwd) | synonymous_variant; upstream_gene_variant | 1 (0/1/0) |
| rs28364996 | chr5:1432686(Fwd) | synonymous_variant | 1 (0/0/1) |
| rs6296 | chr6:78172260(Fwd) | synonymous_variant | 10 (3/7/0) |
| rs1397547 | chr4:62845388(Fwd) | synonymous_variant | 1 (0/0/1) |
| rs6298 | chr6:78172992(Fwd) | synonymous_variant | 4 (0/4/0) |
| rs1805068 | chr16:55727958(Fwd) | synonymous_variant | 1 (0/0/1) |
| rs10434219 | chr4:62598689(Fwd) | synonymous_variant | 1 (0/0/1) |
| rs1042717 | chr5:148206646(Fwd) | synonymous_variant | 1 (1/0/0) |
| rs7305115 | chr12:72372862(Fwd) | synonymous_variant | 1 (0/1/0) |
| rs1397548 | chr4:62845490(Fwd) | splice_region_variant; synonymous_variant | 2 (0/0/2) |
| rs4969349 | chr17:79006033(Fwd) | nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant | 1 (0/1/0) |
| rs34246405 | chr4:62812738(Fwd) | nc_transcript_variant; non_coding_exon_variant; synonymous_variant | 1 (0/0/1) |
| rs734644 | chr4:62800728(Fwd) | nc_transcript_variant; non_coding_exon_variant; synonymous_variant | 1 (0/0/1) |
| rs10013832 | chr4:62800626(Fwd) | nc_transcript_variant; non_coding_exon_variant; synonymous_variant | 1 (0/0/1) |
| rs1137070 | chrX:43603391(Fwd) | nc_transcript_variant; non_coding_exon_variant; synonymous_variant | 4 (3/1/0) |
| rs1326022 | chr20:54844025(Fwd) | nc_transcript_variant; non_coding_exon_variant | 1 (0/1/0) |
| rs3025343 | chr9:136478355(Fwd) | nc_transcript_variant; non_coding_exon_variant | 1 (0/1/0) |
| rs1326021 | chr20:54844146(Fwd) | nc_transcript_variant; non_coding_exon_variant | 1 (0/1/0) |
| rs8005625 | chr14:44010789(Fwd) | nc_transcript_variant; non_coding_exon_variant | 1 (0/1/0) |
| rs4633 | chr22:19950235(Fwd) | nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; synonymous_variant; upstream_gene_variant | 2 (1/1/0) |
| rs1051730 | chr15:78894339(Fwd) | nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; synonymous_variant | 1 (0/1/0) |
| rs28364997 | chr5:1403128(Fwd) | missense_variant; upstream_gene_variant | 1 (0/0/1) |
| rs5522 | chr4:149357475(Fwd) | missense_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs16976466 | chr15:55972797(Fwd) | missense_variant; nc_transcript_variant; non_coding_exon_variant; splice_region_variant; upstream_gene_variant | 1 (0/1/0) |
| rs6271 | chr9:136522274(Fwd) | missense_variant; nc_transcript_variant; non_coding_exon_variant | 1 (0/1/0) |
| rs1805066 | chr16:55719143(Fwd) | missense_variant | 1 (0/0/1) |
| rs1042714 | chr5:148206473(Fwd) | missense_variant | 1 (0/1/0) |
| rs1801253 | chr10:115805056(Fwd) | missense_variant | 1 (0/1/0) |
| rs4504469 | chr6:24588884(Fwd) | missense_variant | 1 (0/1/0) |
| rs6314 | chr13:47409034(Fwd) | missense_variant | 4 (0/4/0) |
| rs1438914 | chr15:55912875(Fwd) | missense_variant | 1 (1/0/0) |
| rs6280 | chr3:113890815(Fwd) | missense_variant | 2 (0/2/0) |
| rs10421632 | chr19:57764770(Fwd) | missense_variant | 1 (0/0/1) |
| rs5320 | chr9:136507473(Fwd) | missense_variant | 1 (1/0/0) |
| rs12509110 | chr4:62845461(Fwd) | missense_variant | 1 (0/0/1) |
| rs6318 | chrX:113965735(Fwd) | missense_variant | 2 (0/2/0) |
| rs130060 | chr6:78172750(Fwd) | missense_variant | 1 (0/1/0) |
| rs10838881 | chr11:48387275(Fwd) | missense_variant | 1 (0/0/1) |
| rs907697 | chr1:202568735(Fwd) | intron_variant; upstream_gene_variant | 1 (1/0/0) |
| rs2242073 | chr2:208994045(Fwd) | intron_variant; upstream_gene_variant | 1 (0/0/1) |
| rs2007494 | chr15:55792245(Fwd) | intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs11564752 | chr5:1444985(Fwd) | intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs7463256 | chr8:23101620(Fwd) | intron_variant; upstream_gene_variant | 1 (0/0/1) |
| rs16928529 | chr10:72982985(Fwd) | intron_variant; upstream_gene_variant | 1 (0/0/1) |
| rs2937639 | chr5:1443728(Fwd) | intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs3808585 | chr8:26724326(Fwd) | intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs41154 | chr16:55702706(Fwd) | intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs4804149 | chr19:11284028(Fwd) | intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs17057305 | chr5:159381080(Fwd) | intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs2502731 | chr9:130976557(Fwd) | intron_variant; upstream_gene_variant | 1 (0/0/1) |
| rs2239448 | chrX:43602679(Fwd) | intron_variant; upstream_gene_variant | 3 (3/0/0) |
| rs9545424 | chr13:36383264(Fwd) | intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs2073837 | chr9:136522928(Fwd) | intron_variant; upstream_gene_variant | 1 (1/0/0) |
| rs12496256 | chr3:32299549(Fwd) | intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs4583306 | chr17:28538715(Fwd) | intron_variant; upstream_gene_variant | 1 (1/0/0) |
| rs1923886 | chr13:47423291(Fwd) | intron_variant; upstream_gene_variant | 1 (1/0/0) |
| rs16880453 | chr5:52195507(Fwd) | intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs3812047 | chr5:37835398(Fwd) | intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs1979398 | chr5:52194327(Fwd) | intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs1316830 | chr5:1443990(Fwd) | intron_variant; upstream_gene_variant | 1 (1/0/0) |
| rs37020 | chr5:1418374(Fwd) | intron_variant; upstream_gene_variant | 2 (1/1/0) |
| rs10786284 | chr10:98135505(Fwd) | intron_variant; upstream_gene_variant | 1 (0/0/1) |
| rs7632299 | chr3:143056467(Fwd) | intron_variant; upstream_gene_variant | 1 (1/0/0) |
| rs1466445 | chr5:52195127(Fwd) | intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs979605 | chrX:43601363(Fwd) | intron_variant; upstream_gene_variant | 2 (0/2/0) |
| rs140701 | chr17:28538532(Fwd) | intron_variant; upstream_gene_variant | 3 (1/2/0) |
| rs994856 | chr13:42708451(Fwd) | intron_variant; upstream_gene_variant | 1 (1/0/0) |
| rs12653825 | chr5:159383271(Fwd) | intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs2072744 | chrX:43599436(Fwd) | intron_variant; upstream_gene_variant | 1 (1/0/0) |
| rs793862 | chr6:24207200(Fwd) | intron_variant; upstream_gene_variant | 1 (1/0/0) |
| rs2797849 | chr9:136501941(Fwd) | intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs2773822 | chr9:135861033(Fwd) | intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs6454674 | chr6:88872930(Fwd) | intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs133945 | chr22:33402843(Fwd) | intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs2267770 | chr16:9865959(Fwd) | intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs11133767 | chr5:1401580(Fwd) | intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs187715 | chr16:55704042(Fwd) | intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs133946 | chr22:33403278(Fwd) | intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs1800887 | chr16:55733589(Fwd) | intron_variant; upstream_gene_variant | 2 (0/2/0) |
| rs1495099 | chr17:37784464(Fwd) | intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs2298122 | chr10:135141572(Fwd) | intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs6313 | chr13:47469940(Fwd) | intron_variant; synonymous_variant | 4 (0/4/0) |
| rs1108580 | chr9:136505114(Fwd) | intron_variant; splice_region_variant; synonymous_variant | 6 (1/5/0) |
| rs7165971 | chr15:55921013(Fwd) | intron_variant; splice_region_variant | 1 (1/0/0) |
| rs358834 | chr4:21549850(Fwd) | intron_variant; NMD_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs1150222 | chr11:113846872(Fwd) | intron_variant; NMD_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs17651978 | chr3:71020490(Fwd) | intron_variant; NMD_transcript_variant; upstream_gene_variant | 1 (0/0/1) |
| rs169806 | chr11:18059292(Fwd) | intron_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs573514 | chr8:26721281(Fwd) | intron_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs6445067 | chr3:165535113(Fwd) | intron_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs1451371 | chr7:50553051(Fwd) | intron_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs3799977 | chr6:44837356(Fwd) | intron_variant; NMD_transcript_variant | 1 (0/0/1) |
| rs7012857 | chr8:120825225(Fwd) | intron_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs12646862 | chr4:21922119(Fwd) | intron_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs876477 | chr4:21156928(Fwd) | intron_variant; NMD_transcript_variant | 2 (0/2/0) |
| rs13317247 | chr3:7026535(Fwd) | intron_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs829508 | chr3:165502724(Fwd) | intron_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs17794760 | chr11:18055920(Fwd) | intron_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs591556 | chr11:18061400(Fwd) | intron_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs4732641 | chr8:26617904(Fwd) | intron_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs6944090 | chr7:50573140(Fwd) | intron_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs10513219 | chr3:143534874(Fwd) | intron_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs11122330 | chr1:231898591(Fwd) | intron_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs13110425 | chr4:21351505(Fwd) | intron_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs7616384 | chr3:143453195(Fwd) | intron_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs6592961 | chr7:50572890(Fwd) | intron_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs7356396 | chr4:21918540(Fwd) | intron_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs11191454 | chr10:104660004(Fwd) | intron_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs10832876 | chr11:18059929(Fwd) | intron_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs6989791 | chr8:120824357(Fwd) | intron_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs7172689 | chr15:81533695(Fwd) | intron_variant; NMD_transcript_variant | 1 (0/0/1) |
| rs1304358 | chr2:198969583(Fwd) | intron_variant; NMD_transcript_variant | 1 (0/0/1) |
| rs2241685 | chr2:1925993(Fwd) | intron_variant; NMD_transcript_variant | 1 (0/0/1) |
| rs2281597 | chr1:34359858(Fwd) | intron_variant; NMD_transcript_variant | 1 (0/0/1) |
| rs528257 | chr8:26721296(Fwd) | intron_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs11606304 | chr11:18052248(Fwd) | intron_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs1278776 | chr13:113520362(Fwd) | intron_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs17817356 | chr1:231920221(Fwd) | intron_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs1470750 | chr7:50576648(Fwd) | intron_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs7657608 | chr4:168154181(Fwd) | intron_variant; NMD_transcript_variant | 2 (0/2/0) |
| rs1538979 | chr1:231896868(Fwd) | intron_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs4128767 | chr15:81543407(Fwd) | intron_variant; NMD_transcript_variant | 1 (0/0/1) |
| rs17689952 | chr4:166939154(Fwd) | intron_variant; NMD_transcript_variant | 2 (0/2/0) |
| rs10488683 | chr11:18053545(Fwd) | intron_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs3776585 | chr5:36668022(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs2237349 | chr7:28762963(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/0/1) |
| rs9842394 | chr3:179613236(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/0/1) |
| rs2394538 | chr10:71033697(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs7928249 | chr11:71161063(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/0/1) |
| rs10807124 | chr6:33404064(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 2 (0/2/0) |
| rs737865 | chr22:19930121(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs7267923 | chr20:61996901(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs6295 | chr5:63258565(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 2 (1/1/0) |
| rs174611 | chr11:61627881(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs2206161 | chr20:10334969(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs1889189 | chr20:10197086(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 3 (0/3/0) |
| rs3818204 | chr20:61991141(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs737866 | chr22:19930109(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs11757000 | chr6:28484869(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs4771122 | chr13:28020180(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs10767664 | chr11:27725986(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 2 (1/1/0) |
| rs933271 | chr22:19931407(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs1079727 | chr11:113289182(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs12514589 | chr5:37842431(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs242089 | chr22:33213319(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs690378 | chr18:74081272(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs3763965 | chr11:27528987(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs6039769 | chr20:10198954(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs4374483 | chr3:125920064(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs362584 | chr20:10254475(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs941298 | chr7:73125263(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs1023556 | chr7:34696545(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs755203 | chr20:61994264(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 2 (1/1/0) |
| rs5993882 | chr22:19937533(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs6077690 | chr20:10197461(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 2 (1/1/0) |
| rs11689432 | chr2:239141505(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs4591778 | chr5:36608165(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs4838721 | chr10:135160950(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs498793 | chr11:61624705(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 2 (1/1/0) |
| rs1799978 | chr11:113346351(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs10042486 | chr5:63261329(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs2305339 | chr4:62800554(Fwd) | intron_variant; nc_transcript_variant; splice_region_variant | 2 (0/0/2) |
| rs6332 | chr12:5603632(Fwd) | intron_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant | 4 (1/3/0) |
| rs2143340 | chr6:24659071(Fwd) | intron_variant; nc_transcript_variant; non_coding_exon_variant | 1 (0/1/0) |
| rs2423486 | chr20:10212212(Fwd) | intron_variant; nc_transcript_variant; non_coding_exon_variant | 2 (0/2/0) |
| rs4913069 | chr5:139545110(Fwd) | intron_variant; nc_transcript_variant; non_coding_exon_variant | 2 (0/2/0) |
| rs2042449 | chr5:1416646(Fwd) | intron_variant; nc_transcript_variant; non_coding_exon_variant | 2 (1/1/0) |
| rs6039806 | chr20:10258654(Fwd) | intron_variant; nc_transcript_variant; non_coding_exon_variant | 3 (1/2/0) |
| rs2073833 | chr9:136520282(Fwd) | intron_variant; nc_transcript_variant; non_coding_exon_variant | 1 (0/1/0) |
| rs10513003 | chr5:52228442(Fwd) | intron_variant; nc_transcript_variant; non_coding_exon_variant | 1 (0/1/0) |
| rs6565531 | chr17:79023380(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs2273505 | chr20:61990878(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 2 (1/1/0) |
| rs6090384 | chr20:61990874(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 4 (0/4/0) |
| rs3787141 | chr20:61989394(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs16870771 | chr4:21307781(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs42259 | chr5:14386655(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (0/0/1) |
| rs11135712 | chr8:23110503(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (0/0/1) |
| rs2322333 | chr8:26695255(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs10503800 | chr8:26695617(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs11657991 | chr17:79029748(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs4969245 | chr17:79056453(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs10228350 | chr7:114060663(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs574647 | chr8:26697057(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs11080121 | chr17:28528842(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs4969385 | chr17:79068890(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs472865 | chr8:26698471(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs2020917 | chr22:19928884(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs740603 | chr22:19945177(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 2 (0/2/0) |
| rs17052671 | chr4:167841284(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs8079626 | chr17:79026872(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs4325622 | chr17:28526475(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs1982406 | chr7:50597627(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs469727 | chr5:112242968(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (0/0/1) |
| rs8067235 | chr17:79024637(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs577366 | chr8:26697365(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs2075507 | chr22:19928092(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs4074905 | chr11:2189185(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs11657536 | chr17:28529242(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs2273506 | chr20:61990939(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; synonymous_variant; upstream_gene_variant | 3 (0/3/0) |
| rs8079781 | chr17:79050148(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant | 1 (1/0/0) |
| rs7660401 | chr4:167780915(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs17137124 | chr7:114210814(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs1229761 | chr7:114223723(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs13114933 | chr4:167865980(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs3743204 | chr15:55790310(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs10025945 | chr4:167823254(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs7660050 | chr4:167959369(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs692691 | chr15:55760575(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs7698061 | chr4:168007813(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs11659017 | chr17:79018379(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs1984895 | chr1:231962297(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs821577 | chr1:232067057(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs11725742 | chr4:167865350(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs4602517 | chr4:167684929(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs13128738 | chr4:167961410(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs17598103 | chr4:167703897(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs1558902 | chr16:53803574(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs1427635 | chr4:167999350(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs13117458 | chr4:168004426(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs10011926 | chr4:111026927(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/0/1) |
| rs2318483 | chr4:167662272(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs1000731 | chr1:231963491(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs17079773 | chr13:24598384(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/0/1) |
| rs11686538 | chr2:225818564(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/0/1) |
| rs7503597 | chr17:79049273(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs1015101 | chr1:232007694(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs1834833 | chr4:167898814(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs3760201 | chr17:21193618(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs10110744 | chr8:26685961(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs897511 | chr4:167695661(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs17702475 | chr4:167901033(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs4727799 | chr7:114110568(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs1349384 | chr4:21762936(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs11191580 | chr10:104906211(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs9637685 | chr4:167715416(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs17702109 | chr4:167797557(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs7940188 | chr11:27693739(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs1551773 | chr4:91856308(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/0/1) |
| rs13102367 | chr4:167883955(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs8050136 | chr16:53816275(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs11097273 | chr4:91828373(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/0/1) |
| rs13113012 | chr4:167810891(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs10150332 | chr14:79936964(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs11629841 | chr15:55777638(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs17696409 | chr4:167704731(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs6822214 | chr4:168011464(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs10018183 | chr4:167715036(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs1593770 | chr4:167902573(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs7340679 | chr3:15346700(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/0/1) |
| rs8045006 | chr16:83256273(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs1349492 | chr7:50546459(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs11722292 | chr4:167954614(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs7689440 | chr4:167685213(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs6565113 | chr16:83107646(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs2199161 | chr5:71410356(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/0/1) |
| rs11779546 | chr8:26674936(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs10486026 | chr7:114080435(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs10268637 | chr7:114074257(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs17052591 | chr4:167693200(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs897514 | chr4:167776873(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs17052602 | chr4:167714310(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs11646411 | chr16:82746937(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/0/1) |
| rs523816 | chr8:26703750(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs6857340 | chr4:167913177(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs7440269 | chr4:167789207(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs10255943 | chr7:114072443(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs2280934 | chr8:23106665(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/0/1) |
| rs12533005 | chr7:114056055(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs7683298 | chr4:168013532(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs7809589 | chr7:151473813(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/0/1) |
| rs2049045 | chr11:27694241(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs922781 | chr15:61070344(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 2 (0/2/0) |
| rs999710 | chr1:232010943(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs3792452 | chr3:7666784(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs7683787 | chr4:91830629(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/0/1) |
| rs4076037 | chr17:79044284(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs732215 | chr7:50544063(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs616668 | chr12:111974280(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/0/1) |
| rs11777551 | chr8:26672727(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs1346376 | chr4:167892885(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs1176717 | chr11:113855342(Fwd) | intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs1705236 | chr12:71545558(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs4689440 | chr4:6421406(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs10892592 | chr11:120522003(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs362555 | chr20:10309836(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs2327265 | chr20:10218274(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs1900633 | chr3:143398098(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs13188662 | chr5:52091647(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs4936537 | chr11:120526365(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs7732839 | chr5:52173770(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs910330 | chr1:115835500(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs2556378 | chr2:60762502(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs363006 | chr20:10280083(Fwd) | intron_variant; nc_transcript_variant | 6 (0/6/0) |
| rs3776576 | chr5:36649627(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs1940028 | chr11:131842743(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs363050 | chr20:10234257(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs4570590 | chr11:120523139(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs3788862 | chrX:43517364(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs4747989 | chr10:12590175(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs790531 | chr13:50725514(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs1242070 | chr3:143370967(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs1491850 | chr11:27749725(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs1421927 | chr5:52242033(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs16889388 | chr4:13893168(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs1428975 | chr5:36623740(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs4813023 | chr20:10194246(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs17729098 | chr20:59077648(Fwd) | intron_variant; nc_transcript_variant | 2 (0/0/2) |
| rs880140 | chr2:239155732(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs6100796 | chr20:58800873(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs2283724 | chrX:43559576(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs1583670 | chr10:132984214(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs1535028 | chr20:58814428(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs12378218 | chr9:120648450(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs1478442 | chr5:52209963(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs4929949 | chr11:8604593(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs2126953 | chr5:52161157(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs2251214 | chr12:79823851(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs12432593 | chr14:34731592(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs1386494 | chr12:72352543(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs4813925 | chr20:10286313(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs1242058 | chr3:143377573(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs10983238 | chr9:119333683(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs2823819 | chr21:17828291(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs1862638 | chr5:36628597(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs11593241 | chr10:132986646(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs4930767 | chr12:5597381(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs1430961 | chr4:90552920(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs7955501 | chr12:72350026(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs2406217 | chr5:52110389(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs3025873 | chr20:10269040(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs9982805 | chr21:23383609(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs12576775 | chr11:79077193(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs8098539 | chr18:11775386(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs13330107 | chr16:76878862(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs13227216 | chr7:128490553(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs7631319 | chr3:143403277(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs9816226 | chr3:185834499(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs11847697 | chr14:30515112(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs2856811 | chr1:115838282(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs1386493 | chr12:72355179(Fwd) | intron_variant; nc_transcript_variant | 5 (2/3/0) |
| rs9962277 | chr18:11799182(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs6582072 | chr12:72354477(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs4549394 | chr4:129431298(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs6537860 | chr1:115856344(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs11727760 | chr4:6352060(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs2893482 | chr7:34629104(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs2172802 | chr4:62453209(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs7958038 | chr12:5576594(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs1242068 | chr3:143371447(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs2865793 | chr20:58799401(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs1744062 | chr6:137309186(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs3776579 | chr5:36654493(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs6108464 | chr20:10283950(Fwd) | intron_variant; nc_transcript_variant | 3 (1/2/0) |
| rs12843268 | chrX:43573666(Fwd) | intron_variant; nc_transcript_variant | 3 (2/1/0) |
| rs6077699 | chr20:10224306(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs11719664 | chr3:21955198(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs6074109 | chr20:10193294(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs1386496 | chr12:72350790(Fwd) | intron_variant; nc_transcript_variant | 2 (0/2/0) |
| rs4964805 | chr12:104192824(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs4935750 | chr11:120521066(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs2033791 | chr10:132993403(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs2295426 | chr14:59376455(Fwd) | intron_variant; nc_transcript_variant | 2 (0/2/0) |
| rs760609 | chr6:114708100(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs2860025 | chr5:52114050(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs3859124 | chr16:10088063(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs2129575 | chr12:72340073(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs4245149 | chr11:113338357(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs6815704 | chr4:93474566(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs3787303 | chr20:10208748(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs4147141 | chr1:69579252(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs1080750 | chr9:34581525(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs2327264 | chr20:10206254(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs719452 | chr1:115837057(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs6462569 | chr7:34638014(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs16917204 | chr11:27668355(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs1843809 | chr12:72348698(Fwd) | intron_variant; nc_transcript_variant | 6 (4/2/0) |
| rs2423487 | chr20:10213095(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs10512416 | chr9:134913378(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs7577925 | chr2:134040519(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs4565946 | chr12:72336769(Fwd) | intron_variant; nc_transcript_variant | 2 (0/2/0) |
| rs237885 | chr3:8795543(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs11030096 | chr11:27665543(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs13353224 | chr18:65400425(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs2114961 | chr5:134574232(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs13316193 | chr3:8802743(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs3788863 | chrX:43524765(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs12679254 | chr8:74274191(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs362988 | chr20:10281370(Fwd) | intron_variant; nc_transcript_variant | 3 (1/2/0) |
| rs7315638 | chr12:79807279(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs53576 | chr3:8804371(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs363040 | chr20:10221467(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs4350392 | chr11:113335717(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs7132127 | chr12:5552076(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs363512 | chr21:31050817(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs363021 | chr20:10241811(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs4624074 | chr14:34744426(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs2360867 | chr3:143405663(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs11786458 | chr8:40252701(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs1242075 | chr3:143366830(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs1245769 | chr12:79776101(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs1370868 | chr10:132984356(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs2327269 | chr20:10303128(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs4642009 | chr20:10267726(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs1938526 | chr10:62300383(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs2397752 | chr10:132983821(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs9350410 | chr6:22033010(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs2601126 | chr3:11036624(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs363039 | chr20:10220496(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs2241423 | chr15:68086838(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs2439832 | chr15:43779686(Fwd) | intron_variant; nc_transcript_variant | 2 (0/2/0) |
| rs6791644 | chr3:60771108(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs362553 | chr20:10299223(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs11625217 | chr14:34728231(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs6039820 | chr20:10282027(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs1623319 | chr12:76270756(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs6828090 | chr4:6459482(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs36051446 | chr3:61603665(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs10258145 | chr7:34599721(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs2061971 | chr10:45089053(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs16838844 | chr4:6440620(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs7495052 | chr15:92552029(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs362562 | chr20:10243186(Fwd) | intron_variant; nc_transcript_variant | 2 (0/2/0) |
| rs11178999 | chr12:72333570(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs10459109 | chr12:126019726(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs5905702 | chrX:43518188(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs363225 | chr10:119024502(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs6732434 | chr2:182901257(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs2193968 | chr5:52247233(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs17023218 | chr3:29342717(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs6104571 | chr20:10224750(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs3903407 | chr5:36656953(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs362567 | chr20:10246091(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs8095592 | chr18:11753716(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs7012077 | chr8:24282721(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs1555322 | chr20:33849179(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs363012 | chr20:10219799(Fwd) | intron_variant; nc_transcript_variant | 2 (0/2/0) |
| rs727605 | chr16:9955564(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs2220330 | chr12:72351708(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs362569 | chr20:10246733(Fwd) | intron_variant; nc_transcript_variant | 3 (0/3/0) |
| rs11790994 | chr9:98429266(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs10748185 | chr12:72335855(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs4245040 | chr11:120520629(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs2323262 | chr4:22144436(Fwd) | intron_variant; nc_transcript_variant | 2 (0/2/0) |
| rs363052 | chr20:10235426(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs1386495 | chr12:72352322(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs2052661 | chr18:11763020(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs362585 | chr20:10256252(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs6539445 | chr12:79763394(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs6610845 | chrX:43588010(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs9525584 | chr13:42734894(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs3779312 | chr7:77711756(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs17722514 | chr13:90713945(Fwd) | intron_variant; nc_transcript_variant | 2 (0/2/0) |
| rs6327 | chr1:115829986(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs11243897 | chr9:135618283(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs4806874 | chr19:2738352(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs12626080 | chr20:10233052(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs363035 | chr20:10218958(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs4421131 | chr5:36685465(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs1242076 | chr3:143366463(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs2076240 | chr20:10264922(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs2254404 | chr1:115834669(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs3741410 | chr11:48168664(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs7175404 | chr15:94036688(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs363014 | chr20:10228694(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs1170101 | chr13:42776055(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs7271202 | chr20:58801643(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs11175219 | chr12:64362719(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs9873087 | chr3:143394491(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs347405 | chr13:42790179(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs2161961 | chr18:11774500(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs3787283 | chr20:10284418(Fwd) | intron_variant; nc_transcript_variant | 3 (1/2/0) |
| rs10132279 | chr14:38533095(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs363020 | chr20:10237223(Fwd) | intron_variant; nc_transcript_variant | 2 (1/1/0) |
| rs7702178 | chr5:172196997(Fwd) | intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs9525580 | chr13:42720699(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs1386488 | chr12:72344618(Fwd) | intron_variant; nc_transcript_variant | 2 (0/2/0) |
| rs6108461 | chr20:10267270(Fwd) | intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs362549 | chr20:10269890(Fwd) | intron_variant; nc_transcript_variant | 3 (2/1/0) |
| rs3782309 | chr12:26859396(Fwd) | intron_variant; nc_transcript_variant | 2 (0/2/0) |
| rs4923705 | chr15:36293605(Fwd) | intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs2032892 | chr5:36677083(Fwd) | intron_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant | 1 (0/1/0) |
| rs1048101 | chr8:26628028(Fwd) | intron_variant; missense_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; upstream_gene_variant | 1 (0/1/0) |
| rs1799971 | chr6:154360797(Fwd) | intron_variant; missense_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant | 1 (1/0/0) |
| rs60593443 | chr8:26636906(Fwd) | intron_variant; missense_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs324981 | chr7:34818113(Fwd) | intron_variant; missense_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs6330 | chr1:115829313(Fwd) | intron_variant; missense_variant; nc_transcript_variant | 1 (0/1/0) |
| rs1550326 | chr15:55933199(Fwd) | intron_variant | 1 (0/1/0) |
| rs6582081 | chr12:72383614(Fwd) | intron_variant | 1 (1/0/0) |
| rs765287 | chr16:9876382(Fwd) | intron_variant | 1 (0/1/0) |
| rs13115125 | chr4:62867453(Fwd) | intron_variant | 1 (1/0/0) |
| rs1328684 | chr13:47466230(Fwd) | intron_variant | 1 (1/0/0) |
| rs13162302 | chr5:159367275(Fwd) | intron_variant | 1 (0/1/0) |
| rs6706295 | chr2:226364934(Fwd) | intron_variant | 1 (0/1/0) |
| rs1108581 | chr9:136505241(Fwd) | intron_variant | 1 (0/1/0) |
| rs7963226 | chr12:72365866(Fwd) | intron_variant | 1 (1/0/0) |
| rs2284411 | chr12:13866172(Fwd) | intron_variant | 2 (1/1/0) |
| rs7990263 | chr13:36461216(Fwd) | intron_variant | 1 (0/1/0) |
| rs10823978 | chr10:53787957(Fwd) | intron_variant | 1 (0/1/0) |
| rs4765913 | chr12:2419896(Fwd) | intron_variant | 1 (0/1/0) |
| rs4760820 | chr12:72396996(Fwd) | intron_variant | 1 (0/1/0) |
| rs987237 | chr6:50803050(Fwd) | intron_variant | 1 (1/0/0) |
| rs4760818 | chr12:72378923(Fwd) | intron_variant | 2 (1/1/0) |
| rs11568324 | chr16:55726058(Fwd) | intron_variant | 5 (4/1/0) |
| rs393795 | chr5:1428514(Fwd) | intron_variant | 1 (0/1/0) |
| rs6084670 | chr20:4222509(Fwd) | intron_variant | 1 (0/1/0) |
| rs36017 | chr16:55718818(Fwd) | intron_variant | 2 (0/2/0) |
| rs16965628 | chr17:28555425(Fwd) | intron_variant | 1 (0/1/0) |
| rs1386498 | chr12:72398143(Fwd) | intron_variant | 1 (0/1/0) |
| rs1011061 | chr15:55987498(Fwd) | intron_variant | 1 (0/1/0) |
| rs2122643 | chr4:62654938(Fwd) | intron_variant | 1 (1/0/0) |
| rs11953346 | chr5:94141447(Fwd) | intron_variant | 1 (0/1/0) |
| rs36021 | chr16:55711950(Fwd) | intron_variant | 3 (1/2/0) |
| rs17306977 | chr16:55693373(Fwd) | intron_variant | 1 (0/1/0) |
| rs1862574 | chr5:37830577(Fwd) | intron_variant | 1 (0/1/0) |
| rs3776513 | chr5:1407104(Fwd) | intron_variant | 2 (2/0/0) |
| rs16902086 | chr5:45285752(Fwd) | intron_variant | 1 (0/1/0) |
| rs1023990 | chr12:72382247(Fwd) | intron_variant | 1 (0/1/0) |
| rs17268988 | chrX:7254481(Fwd) | intron_variant | 1 (0/1/0) |
| rs787558 | chr18:11865878(Fwd) | intron_variant | 1 (0/1/0) |
| rs10823964 | chr10:53777043(Fwd) | intron_variant | 1 (0/0/1) |
| rs7322347 | chr13:47410103(Fwd) | intron_variant | 1 (1/0/0) |
| rs17151821 | chr7:8628491(Fwd) | intron_variant | 1 (0/1/0) |
| rs1549250 | chr5:37821221(Fwd) | intron_variant | 1 (0/1/0) |
| rs690111 | chr9:93377290(Fwd) | intron_variant | 1 (0/1/0) |
| rs7816032 | chr8:19786891(Fwd) | intron_variant | 1 (0/0/1) |
| rs7984422 | chr13:92808689(Fwd) | intron_variant | 1 (0/0/1) |
| rs1386497 | chr12:72392290(Fwd) | intron_variant | 2 (1/1/0) |
| rs2770296 | chr13:47440560(Fwd) | intron_variant | 1 (1/0/0) |
| rs10278591 | chr7:1921362(Fwd) | intron_variant | 1 (0/1/0) |
| rs11179027 | chr12:72377312(Fwd) | intron_variant | 1 (1/0/0) |
| rs17722134 | chr12:72401694(Fwd) | intron_variant | 1 (0/1/0) |
| rs2290070 | chr5:44305309(Fwd) | intron_variant | 1 (0/1/0) |
| rs2205718 | chrX:43597465(Fwd) | intron_variant | 1 (0/1/0) |
| rs167771 | chr3:113876275(Fwd) | intron_variant | 1 (0/1/0) |
| rs17495366 | chr2:50268616(Fwd) | intron_variant | 1 (0/1/0) |
| rs12591646 | chr15:55919139(Fwd) | intron_variant | 1 (1/0/0) |
| rs6133098 | chr20:4217249(Fwd) | intron_variant | 1 (0/1/0) |
| rs5934740 | chrX:7157652(Fwd) | intron_variant | 2 (0/2/0) |
| rs1406946 | chr6:87647591(Fwd) | intron_variant | 1 (1/0/0) |
| rs2873804 | chr9:136505644(Fwd) | intron_variant | 1 (0/1/0) |
| rs2981359 | chr5:1442732(Fwd) | intron_variant | 1 (0/1/0) |
| rs4760814 | chr12:72366934(Fwd) | intron_variant | 1 (0/1/0) |
| rs429699 | chr5:1409127(Fwd) | intron_variant | 1 (1/0/0) |
| rs13119057 | chr4:46807501(Fwd) | intron_variant | 1 (0/1/0) |
| rs4939921 | chr18:47462328(Fwd) | intron_variant | 1 (0/1/0) |
| rs1331503 | chr9:93402517(Fwd) | intron_variant | 1 (1/0/0) |
| rs16938747 | chr8:74879087(Fwd) | intron_variant | 1 (0/0/1) |
| rs994092 | chr5:45335759(Fwd) | intron_variant | 1 (0/1/0) |
| rs1000900 | chrX:7152113(Fwd) | intron_variant | 1 (0/1/0) |
| rs11795386 | chr9:87602898(Fwd) | intron_variant | 1 (1/0/0) |
| rs934886 | chr15:55939959(Fwd) | intron_variant | 1 (0/1/0) |
| rs1926452 | chr13:36444937(Fwd) | intron_variant | 1 (0/1/0) |
| rs6551665 | chr4:62739541(Fwd) | intron_variant | 1 (1/0/0) |
| rs6803740 | chr3:32344306(Fwd) | intron_variant | 1 (1/0/0) |
| rs1541665 | chr5:170142917(Fwd) | intron_variant | 2 (0/2/0) |
| rs7183943 | chr15:55875066(Fwd) | intron_variant | 1 (0/1/0) |
| rs10507435 | chr13:36440996(Fwd) | intron_variant | 1 (1/0/0) |
| rs2235185 | chrX:43595743(Fwd) | intron_variant | 1 (1/0/0) |
| rs7164335 | chr15:68715032(Fwd) | intron_variant | 1 (0/0/1) |
| rs7901487 | chr10:53789388(Fwd) | intron_variant | 1 (0/1/0) |
| rs3785155 | chr16:55722390(Fwd) | intron_variant | 1 (0/1/0) |
| rs10823954 | chr10:53773365(Fwd) | intron_variant | 1 (0/1/0) |
| rs12466468 | chr2:226382951(Fwd) | intron_variant | 1 (0/1/0) |
| rs10994336 | chr10:62179812(Fwd) | intron_variant | 2 (0/2/0) |
| rs874836 | chr22:17301843(Fwd) | intron_variant | 1 (0/0/1) |
| rs40184 | chr5:1395077(Fwd) | intron_variant | 7 (2/5/0) |
| rs17095690 | chr1:75106741(Fwd) | intron_variant | 1 (0/1/0) |
| rs1545285 | chr9:87542369(Fwd) | intron_variant | 1 (1/0/0) |
| rs11095437 | chrX:7165491(Fwd) | intron_variant | 1 (0/1/0) |
| rs8076005 | chr17:28547210(Fwd) | intron_variant | 1 (1/0/0) |
| rs1387926 | chr9:87632663(Fwd) | intron_variant | 1 (1/0/0) |
| rs5016282 | chr11:88741660(Fwd) | intron_variant | 1 (0/0/1) |
| rs140700 | chr17:28543389(Fwd) | intron_variant | 1 (1/0/0) |
| rs192303 | chr16:55700224(Fwd) | intron_variant | 2 (0/2/0) |
| rs324029 | chr3:113881623(Fwd) | intron_variant | 1 (0/1/0) |
| rs1006737 | chr12:2345295(Fwd) | intron_variant | 1 (0/1/0) |
| rs10879357 | chr12:72414563(Fwd) | intron_variant | 1 (0/1/0) |
| rs6657749 | chr1:214576513(Fwd) | intron_variant | 2 (0/2/0) |
| rs2066713 | chr17:28551665(Fwd) | intron_variant | 3 (1/2/0) |
| rs1868790 | chr4:62694717(Fwd) | intron_variant | 1 (1/0/0) |
| rs4764031 | chr12:13889573(Fwd) | intron_variant | 1 (0/1/0) |
| rs2051090 | chr13:36454193(Fwd) | intron_variant | 1 (0/1/0) |
| rs3985768 | chr15:55997544(Fwd) | intron_variant | 1 (0/1/0) |
| rs13078807 | chr3:85884150(Fwd) | intron_variant | 1 (1/0/0) |
| rs1903977 | chr10:53776286(Fwd) | intron_variant | 1 (0/0/1) |
| rs12518844 | chr5:37832759(Fwd) | intron_variant | 1 (0/1/0) |
| rs6892282 | chr5:159360485(Fwd) | intron_variant | 1 (0/1/0) |
| rs3893215 | chr11:17764830(Fwd) | intron_variant | 1 (0/1/0) |
| rs5564 | chr16:55725975(Fwd) | intron_variant | 1 (0/1/0) |
| rs1344706 | chr2:185778428(Fwd) | intron_variant | 2 (0/2/0) |
| rs11764590 | chr7:2032803(Fwd) | intron_variant | 1 (0/1/0) |
| rs2030373 | chr5:159347481(Fwd) | intron_variant | 1 (0/1/0) |
| rs1903960 | chr10:53721176(Fwd) | intron_variant | 1 (0/1/0) |
| rs8183794 | chr20:4210448(Fwd) | intron_variant | 1 (0/1/0) |
| rs2910797 | chr5:37820365(Fwd) | intron_variant | 1 (0/1/0) |
| rs2107281 | chr7:8636552(Fwd) | intron_variant | 1 (0/1/0) |
| rs7722380 | chr5:45678378(Fwd) | intron_variant | 1 (0/1/0) |
| rs2216711 | chr5:37828844(Fwd) | intron_variant | 1 (0/1/0) |
| rs2284407 | chr12:13842206(Fwd) | intron_variant | 1 (1/0/0) |
| rs12438177 | chr15:55951432(Fwd) | intron_variant | 1 (0/1/0) |
| rs6597539 | chr9:134826121(Fwd) | intron_variant | 1 (0/1/0) |
| rs180045 | chr5:178639086(Fwd) | intron_variant | 1 (0/1/0) |
| rs10857701 | chr10:135145072(Fwd) | intron_variant | 1 (0/1/0) |
| rs640401 | chr18:56966832(Fwd) | intron_variant | 1 (1/0/0) |
| rs12110170 | chr5:52142544(Fwd) | intron_variant | 1 (0/1/0) |
| rs6052456 | chr20:4225573(Fwd) | intron_variant | 1 (0/1/0) |
| rs73823293 | chr4:62864014(Fwd) | intron_variant | 1 (0/0/1) |
| rs3787442 | chr20:4225394(Fwd) | intron_variant | 1 (0/1/0) |
| rs1170169 | chr13:42697807(Fwd) | intron_variant | 1 (1/0/0) |
| rs11692499 | chr2:226364402(Fwd) | intron_variant | 1 (0/1/0) |
| rs12053018 | chr2:226395276(Fwd) | intron_variant | 1 (0/1/0) |
| rs7058445 | chrX:7172508(Fwd) | intron_variant | 2 (0/2/0) |
| rs1345429 | chr16:55722850(Fwd) | intron_variant | 1 (0/1/0) |
| rs6858066 | chr4:62754320(Fwd) | intron_variant | 1 (1/0/0) |
| rs1814269 | chr16:55717028(Fwd) | intron_variant | 2 (0/2/0) |
| rs12194307 | chr6:24625562(Fwd) | intron_variant | 1 (0/1/0) |
| rs787554 | chr18:11862697(Fwd) | intron_variant | 1 (0/1/0) |
| rs2020936 | chr17:28550814(Fwd) | intron_variant | 1 (0/1/0) |
| rs10879358 | chr12:72415870(Fwd) | intron_variant | 1 (0/1/0) |
| rs6713607 | chr2:226372129(Fwd) | intron_variant | 1 (0/1/0) |
| rs2973050 | chr5:37817344(Fwd) | intron_variant | 1 (0/1/0) |
| rs5934770 | chrX:7169546(Fwd) | intron_variant | 1 (1/0/0) |
| rs807701 | chr6:24273791(Fwd) | intron_variant | 1 (1/0/0) |
| rs2589162 | chr5:45655893(Fwd) | intron_variant | 1 (0/1/0) |
| rs12920919 | chr16:9937980(Fwd) | intron_variant | 1 (0/1/0) |
| rs2148004 | chr13:42697839(Fwd) | intron_variant | 1 (0/1/0) |
| rs6884105 | chr5:159348443(Fwd) | intron_variant | 1 (0/1/0) |
| rs13395022 | chr2:79882260(Fwd) | intron_variant | 1 (0/1/0) |
| rs10823973 | chr10:53779480(Fwd) | intron_variant | 1 (0/0/1) |
| rs478597 | chr12:117751425(Fwd) | intron_variant | 1 (0/0/1) |
| rs1048953 | chr5:1438174(Fwd) | intron_variant | 1 (0/1/0) |
| rs2602381 | chr2:234584324(Fwd) | intron_variant | 1 (0/0/1) |
| rs756275 | chr5:159351460(Fwd) | intron_variant | 1 (0/1/0) |
| rs10762524 | chr10:53773912(Fwd) | intron_variant | 1 (0/0/1) |
| rs6561333 | chr13:47420312(Fwd) | intron_variant | 2 (2/0/0) |
| rs1391983 | chr5:52129212(Fwd) | intron_variant | 1 (0/1/0) |
| rs6479643 | chr9:136514668(Fwd) | intron_variant | 1 (0/1/0) |
| rs463379 | chr5:1431164(Fwd) | intron_variant | 3 (1/2/0) |
| rs515910 | chr10:105966404(Fwd) | intron_variant | 1 (0/0/1) |
| rs3785151 | chr16:55712519(Fwd) | intron_variant | 1 (0/1/0) |
| rs1354348 | chr3:113906226(Fwd) | intron_variant | 1 (0/1/0) |
| rs1885303 | chr20:4794243(Fwd) | intron_variant | 1 (0/1/0) |
| rs11186320 | chr10:92576448(Fwd) | intron_variant | 1 (1/0/0) |
| rs6888306 | chr5:159367114(Fwd) | intron_variant | 1 (1/0/0) |
| rs10968576 | chr9:28414339(Fwd) | intron_variant | 1 (0/1/0) |
| rs403636 | chr5:1438354(Fwd) | intron_variant | 3 (1/2/0) |
| rs10998087 | chr10:53316743(Fwd) | intron_variant | 1 (0/1/0) |
| rs12259062 | chr10:92610045(Fwd) | intron_variant | 1 (1/0/0) |
| rs2617605 | chr5:1442521(Fwd) | intron_variant | 1 (0/1/0) |
| rs9929758 | chr16:84430781(Fwd) | intron_variant | 1 (0/1/0) |
| rs6440161 | chr3:143019984(Fwd) | intron_variant | 1 (1/0/0) |
| rs7731209 | chr5:37816845(Fwd) | intron_variant | 1 (0/1/0) |
| rs9848371 | chr3:143014479(Fwd) | intron_variant | 1 (1/0/0) |
| rs12213672 | chr6:24628679(Fwd) | intron_variant | 1 (0/1/0) |
| rs17281813 | chr16:49750790(Fwd) | intron_variant | 1 (0/0/1) |
| rs6547829 | chr2:28323869(Fwd) | intron_variant | 1 (1/0/0) |
| rs552655 | chr6:13370488(Fwd) | intron_variant | 1 (1/0/0) |
| rs1539549 | chr13:36451881(Fwd) | intron_variant | 2 (0/2/0) |
| rs4860106 | chr4:62850522(Fwd) | intron_variant | 1 (1/0/0) |
| rs2939678 | chr8:56247138(Fwd) | intron_variant | 2 (0/2/0) |
| rs10879354 | chr12:72409782(Fwd) | intron_variant | 1 (0/1/0) |
| rs2423037 | chr20:4794989(Fwd) | intron_variant | 1 (0/1/0) |
| rs2636788 | chr10:98876941(Fwd) | intron_variant | 1 (0/0/1) |
| rs2973041 | chr5:37830326(Fwd) | intron_variant | 1 (0/1/0) |
| rs1487278 | chr12:72400851(Fwd) | intron_variant | 1 (1/0/0) |
| rs7197278 | chr16:9907064(Fwd) | intron_variant | 1 (0/1/0) |
| rs7997012 | chr13:47411985(Fwd) | intron_variant | 1 (1/0/0) |
| rs2509689 | chr11:102368719(Fwd) | intron_variant | 1 (0/0/1) |
| rs10521329 | chr16:55720458(Fwd) | intron_variant | 2 (0/2/0) |
| rs7327771 | chr13:36679512(Fwd) | intron_variant | 1 (0/1/0) |
| rs36020 | chr16:55713088(Fwd) | intron_variant | 1 (0/1/0) |
| rs11743392 | chr5:45614975(Fwd) | intron_variant | 1 (0/1/0) |
| rs4251417 | chr17:28551858(Fwd) | intron_variant | 1 (0/1/0) |
| rs6793522 | chr3:143150027(Fwd) | intron_variant | 1 (1/0/0) |
| rs3788459 | chr22:32966495(Fwd) | intron_variant | 1 (0/1/0) |
| rs2268115 | chr12:13869725(Fwd) | intron_variant | 1 (1/0/0) |
| rs11101694 | chr10:135146714(Fwd) | intron_variant | 1 (0/1/0) |
| rs1352250 | chr12:72397784(Fwd) | intron_variant | 2 (1/1/0) |
| rs464049 | chr5:1423905(Fwd) | intron_variant | 1 (0/1/0) |
| rs11615016 | chr12:72415994(Fwd) | intron_variant | 1 (0/1/0) |
| rs7092969 | chr10:53707749(Fwd) | intron_variant | 1 (0/0/1) |
| rs891585 | chr2:226400416(Fwd) | intron_variant | 1 (0/1/0) |
| rs1548364 | chr9:136507742(Fwd) | intron_variant | 2 (0/2/0) |
| rs220470 | chr17:3664975(Fwd) | intron_variant | 1 (0/0/1) |
| rs4948418 | chr10:62185494(Fwd) | intron_variant | 1 (0/1/0) |
| rs1532701 | chr16:55698027(Fwd) | intron_variant | 1 (0/1/0) |
| rs4469933 | chr12:72414717(Fwd) | intron_variant | 1 (0/1/0) |
| rs7989807 | chr13:36625089(Fwd) | intron_variant | 1 (1/0/0) |
| rs2270112 | chrX:7170925(Fwd) | intron_variant | 2 (2/0/0) |
| rs7995215 | chr13:94408506(Fwd) | intron_variant | 1 (0/0/1) |
| rs9973180 | chr18:56954214(Fwd) | intron_variant | 2 (0/2/0) |
| rs11953285 | chr5:159391811(Fwd) | intron_variant | 1 (0/1/0) |
| rs7954568 | chr12:72376478(Fwd) | intron_variant | 1 (1/0/0) |
| rs1487276 | chr12:72405059(Fwd) | intron_variant | 1 (1/0/0) |
| rs1070503 | chr16:10265174(Fwd) | intron_variant | 1 (0/1/0) |
| rs7176964 | chr15:87441734(Fwd) | intron_variant | 1 (0/0/1) |
| rs12874830 | chr13:36572040(Fwd) | intron_variant | 1 (1/0/0) |
| rs2242447 | chr16:55735912(Fwd) | intron_variant | 7 (2/5/0) |
| rs3785143 | chr16:55695106(Fwd) | intron_variant | 6 (5/1/0) |
| rs11071200 | chr15:55950082(Fwd) | intron_variant | 1 (1/0/0) |
| rs7893146 | chr10:53772799(Fwd) | intron_variant | 1 (0/1/0) |
| rs6116268 | chr20:4211440(Fwd) | intron_variant | 1 (0/1/0) |
| rs17455703 | chr14:33489372(Fwd) | intron_variant | 1 (1/0/0) |
| rs226082 | chr3:113881013(Fwd) | intron_variant | 1 (0/1/0) |
| rs7999483 | chr13:36353437(Fwd) | intron_variant | 1 (0/1/0) |
| rs8049681 | chr16:55735350(Fwd) | intron_variant | 1 (0/1/0) |
| rs6806500 | chr3:143013203(Fwd) | intron_variant | 1 (1/0/0) |
| rs980510 | chr5:44318532(Fwd) | intron_variant | 1 (0/1/0) |
| rs10503024 | chr18:56975671(Fwd) | intron_variant | 1 (1/0/0) |
| rs2311120 | chr18:52477123(Fwd) | intron_variant | 2 (0/2/0) |
| rs17712565 | chr14:86053777(Fwd) | intron_variant | 1 (0/1/0) |
| rs17110690 | chr12:72407997(Fwd) | intron_variant | 1 (0/1/0) |
| rs8118409 | chr20:4216663(Fwd) | intron_variant | 1 (0/1/0) |
| rs3787441 | chr20:4205060(Fwd) | intron_variant | 1 (0/1/0) |
| rs17335568 | chrX:7174813(Fwd) | intron_variant | 1 (1/0/0) |
| rs10835188 | chr11:27523186(Fwd) | intron_variant | 1 (1/0/0) |
| rs2134655 | chr3:113858201(Fwd) | intron_variant | 1 (0/1/0) |
| rs2284416 | chr12:13919214(Fwd) | intron_variant | 1 (0/1/0) |
| rs2345039 | chr4:62765030(Fwd) | intron_variant | 1 (1/0/0) |
| rs1903979 | chr10:53774826(Fwd) | intron_variant | 1 (0/1/0) |
| rs2268097 | chr12:13752832(Fwd) | intron_variant | 1 (0/1/0) |
| rs2024159 | chrX:7166212(Fwd) | intron_variant | 1 (0/1/0) |
| rs11852746 | chr15:55984265(Fwd) | intron_variant | 1 (0/1/0) |
| rs3782025 | chr11:113807607(Fwd) | intron_variant | 1 (1/0/0) |
| rs1487279 | chr12:72419306(Fwd) | intron_variant | 1 (1/0/0) |
| rs2799573 | chr10:18601928(Fwd) | intron_variant | 1 (1/0/0) |
| rs6561332 | chr13:47419820(Fwd) | intron_variant | 1 (1/0/0) |
| rs6561686 | chr13:53289094(Fwd) | intron_variant | 1 (0/1/0) |
| rs9659997 | chr1:20002518(Fwd) | intron_variant | 1 (1/0/0) |
| rs558290 | chr15:55927698(Fwd) | intron_variant | 1 (0/1/0) |
| rs10762540 | chr10:53789667(Fwd) | intron_variant | 1 (0/1/0) |
| rs10879352 | chr12:72406958(Fwd) | intron_variant | 1 (1/0/0) |
| rs2414424 | chr15:56000063(Fwd) | intron_variant | 1 (1/0/0) |
| rs1514175 | chr1:74991644(Fwd) | intron_variant | 1 (0/1/0) |
| rs5934769 | chrX:7169518(Fwd) | intron_variant | 1 (1/0/0) |
| rs3812463 | chr8:120852100(Fwd) | intron_variant | 1 (0/1/0) |
| rs985409 | chr7:104171423(Fwd) | intron_variant | 1 (1/0/0) |
| rs2297354 | chr9:93404340(Fwd) | intron_variant | 1 (0/1/0) |
| rs2020942 | chr17:28546914(Fwd) | intron_variant | 2 (0/2/0) |
| rs4774800 | chr15:55950941(Fwd) | intron_variant | 1 (0/1/0) |
| rs1750921 | chr13:36452069(Fwd) | intron_variant | 1 (0/1/0) |
| rs36030 | chr16:55693290(Fwd) | intron_variant | 1 (0/1/0) |
| rs4815670 | chr20:4216864(Fwd) | intron_variant | 1 (0/1/0) |
| rs40147 | chr16:55716840(Fwd) | intron_variant | 1 (0/1/0) |
| rs1202199 | chr6:20156174(Fwd) | intron_variant | 1 (0/0/1) |
| rs56038622 | chr4:62861964(Fwd) | intron_variant | 1 (0/0/1) |
| rs11594082 | chr10:73299253(Fwd) | intron_variant | 1 (0/1/0) |
| rs6469849 | chr8:120857169(Fwd) | intron_variant | 1 (0/1/0) |
| rs1007023 | chr12:72388374(Fwd) | intron_variant | 1 (1/0/0) |
| rs7638876 | chr3:113894300(Fwd) | intron_variant | 1 (1/0/0) |
| rs1947274 | chr4:62744240(Fwd) | intron_variant | 1 (1/0/0) |
| rs3785152 | chr16:55716550(Fwd) | intron_variant | 2 (0/2/0) |
| rs1799836 | chrX:43627999(Fwd) | intron_variant | 2 (1/1/0) |
| rs6497730 | chr16:10245670(Fwd) | intron_variant | 1 (0/1/0) |
| rs1017753 | chr9:93377901(Fwd) | intron_variant | 1 (0/1/0) |
| rs1012053 | chr13:42653437(Fwd) | intron_variant | 1 (0/1/0) |
| rs1859156 | chr4:95834034(Fwd) | intron_variant | 1 (0/0/1) |
| rs1556832 | chr20:4215557(Fwd) | intron_variant | 1 (0/1/0) |
| rs13189021 | chr5:1442842(Fwd) | intron_variant | 1 (1/0/0) |
| rs4403552 | chrX:7243304(Fwd) | intron_variant | 1 (0/1/0) |
| rs2300256 | chr12:13868410(Fwd) | intron_variant | 1 (0/1/0) |
| rs6935076 | chr6:24644322(Fwd) | intron_variant | 1 (0/1/0) |
| rs6639786 | chrX:7161475(Fwd) | intron_variant | 1 (1/0/0) |
| rs1487275 | chr12:72410292(Fwd) | intron_variant | 4 (1/3/0) |
| rs6832751 | chr4:814080(Fwd) | intron_variant | 1 (1/0/0) |
| rs1170191 | chr13:42675493(Fwd) | intron_variant | 1 (0/1/0) |
| rs206936 | chr6:34302869(Fwd) | intron_variant | 1 (1/0/0) |
| rs1672717 | chr11:113812733(Fwd) | intron_variant | 2 (2/0/0) |
| rs952037 | chr5:159390877(Fwd) | intron_variant | 2 (1/1/0) |
| rs7737796 | chr5:159369429(Fwd) | intron_variant | 1 (1/0/0) |
| rs10762539 | chr10:53788881(Fwd) | intron_variant | 1 (0/1/0) |
| rs12231356 | chr12:72409548(Fwd) | intron_variant | 1 (0/1/0) |
| rs9312082 | chr4:62599289(Fwd) | intron_variant | 1 (0/0/1) |
| rs11743802 | chr5:44351154(Fwd) | intron_variant | 1 (0/1/0) |
| rs12861247 | chrX:7174199(Fwd) | intron_variant | 3 (2/1/0) |
| rs28364999 | chr5:1400999(Fwd) | feature_truncation; intron_variant | 1 (0/0/1) |
| rs583668 | chr16:33967254(Fwd); chr2:133009053(Rev); chrY:10039596(Fwd) | downstream_gene_variant; upstream_gene_variant; intron_variant; nc_transcript_variant | 3 (2/1/0) |
| rs2842643 | chr6:41650736(Fwd) | downstream_gene_variant; upstream_gene_variant | 1 (0/0/1) |
| rs9832471 | chr3:143570871(Fwd) | downstream_gene_variant; upstream_gene_variant | 1 (1/0/0) |
| rs879606 | chr17:37781849(Fwd) | downstream_gene_variant; upstream_gene_variant | 1 (0/1/0) |
| rs9870661 | chr3:143571267(Fwd) | downstream_gene_variant; upstream_gene_variant | 1 (1/0/0) |
| rs2747100 | chr14:58464986(Fwd) | downstream_gene_variant; upstream_gene_variant | 2 (0/2/0) |
| rs2394534 | chr10:71029302(Fwd) | downstream_gene_variant; upstream_gene_variant | 1 (0/1/0) |
| rs3733358 | chr4:778599(Fwd) | downstream_gene_variant; upstream_gene_variant | 1 (1/0/0) |
| rs7359397 | chr16:28885659(Fwd) | downstream_gene_variant; upstream_gene_variant | 1 (0/1/0) |
| rs4626538 | chr7:129413188(Fwd) | downstream_gene_variant; upstream_gene_variant | 1 (0/1/0) |
| rs5906754 | chrX:49060227(Fwd) | downstream_gene_variant; upstream_gene_variant | 3 (3/0/0) |
| rs7618915 | chr3:52279594(Fwd) | downstream_gene_variant; upstream_gene_variant | 1 (0/1/0) |
| rs412050 | chr22:22307519(Fwd) | downstream_gene_variant; upstream_gene_variant | 1 (0/0/1) |
| rs8142185 | chr22:38451080(Fwd) | downstream_gene_variant; upstream_gene_variant | 1 (0/1/0) |
| rs4686673 | chr3:193861242(Fwd) | downstream_gene_variant; upstream_gene_variant | 1 (1/0/0) |
| rs2934966 | chr17:37824138(Fwd) | downstream_gene_variant; upstream_gene_variant | 2 (2/0/0) |
| rs5569 | chr16:55731835(Fwd) | downstream_gene_variant; synonymous_variant; upstream_gene_variant | 6 (1/4/1) |
| rs11854213 | chr15:55970041(Fwd) | downstream_gene_variant; synonymous_variant; upstream_gene_variant | 1 (0/1/0) |
| rs1053651 | chr17:37822311(Fwd) | downstream_gene_variant; synonymous_variant; upstream_gene_variant | 1 (0/1/0) |
| rs6347 | chr5:1411412(Fwd) | downstream_gene_variant; synonymous_variant | 6 (0/6/0) |
| rs3734973 | chr7:128484816(Fwd) | downstream_gene_variant; synonymous_variant | 1 (0/0/1) |
| rs2229193 | chr16:9943666(Fwd) | downstream_gene_variant; synonymous_variant | 2 (0/2/0) |
| rs6275 | chr11:113283477(Fwd) | downstream_gene_variant; synonymous_variant | 2 (0/2/0) |
| rs77905 | chr9:136518097(Fwd) | downstream_gene_variant; synonymous_variant | 1 (0/1/0) |
| rs6323 | chrX:43591036(Fwd) | downstream_gene_variant; synonymous_variant | 3 (0/3/0) |
| rs11954894 | chr5:50674131(Fwd) | downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant | 1 (0/1/0) |
| rs2228607 | chr7:73122923(Fwd) | downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant; upstream_gene_variant | 1 (1/0/0) |
| rs957795 | chr21:46758719(Fwd) | downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant | 2 (0/2/0) |
| rs10491412 | chr5:50671121(Fwd) | downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant | 1 (0/1/0) |
| rs4818 | chr22:19951207(Fwd) | downstream_gene_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; synonymous_variant; upstream_gene_variant | 3 (2/1/0) |
| rs2073748 | chr22:19968971(Fwd) | downstream_gene_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant | 1 (0/1/0) |
| rs2240717 | chr22:19969106(Fwd) | downstream_gene_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant | 1 (0/1/0) |
| rs4680 | chr22:19951271(Fwd) | downstream_gene_variant; missense_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; upstream_gene_variant | 23 (4/19/0) |
| rs1801133 | chr1:11856378(Fwd) | downstream_gene_variant; missense_variant | 1 (0/1/0) |
| rs13107325 | chr4:103188709(Fwd) | downstream_gene_variant; missense_variant | 1 (0/1/0) |
| rs1800497 | chr11:113270828(Fwd) | downstream_gene_variant; missense_variant | 2 (2/0/0) |
| rs1801131 | chr1:11854476(Fwd) | downstream_gene_variant; missense_variant | 1 (0/1/0) |
| rs3785157 | chr16:55729836(Fwd) | downstream_gene_variant; intron_variant; upstream_gene_variant | 5 (3/2/0) |
| rs998424 | chr16:55731946(Fwd) | downstream_gene_variant; intron_variant; upstream_gene_variant | 7 (2/5/0) |
| rs12244716 | chr10:135128382(Fwd) | downstream_gene_variant; intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs12422045 | chr11:71154820(Fwd) | downstream_gene_variant; intron_variant; upstream_gene_variant | 1 (0/0/1) |
| rs8047672 | chr16:55731735(Fwd) | downstream_gene_variant; intron_variant; upstream_gene_variant | 2 (1/1/0) |
| rs5568 | chr16:55730124(Fwd) | downstream_gene_variant; intron_variant; upstream_gene_variant | 2 (0/2/0) |
| rs1005270 | chr18:11750822(Fwd) | downstream_gene_variant; intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs2070762 | chr11:2186335(Fwd) | downstream_gene_variant; intron_variant; upstream_gene_variant | 2 (1/1/0) |
| rs9804190 | chr10:61839831(Fwd) | downstream_gene_variant; intron_variant; upstream_gene_variant | 1 (0/1/0) |
| rs1573643 | chr15:91420973(Fwd) | downstream_gene_variant; intron_variant; upstream_gene_variant | 1 (0/0/1) |
| rs11603330 | chr11:71153459(Fwd) | downstream_gene_variant; intron_variant; upstream_gene_variant | 1 (0/0/1) |
| rs36009 | chr16:55732620(Fwd) | downstream_gene_variant; intron_variant; upstream_gene_variant | 3 (1/2/0) |
| rs3892113 | chr18:11876613(Fwd) | downstream_gene_variant; intron_variant; splice_region_variant | 1 (0/1/0) |
| rs1800532 | chr11:18047816(Fwd) | downstream_gene_variant; intron_variant; NMD_transcript_variant; upstream_gene_variant | 3 (1/2/0) |
| rs580739 | chr8:26713707(Fwd) | downstream_gene_variant; intron_variant; NMD_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs13274396 | chr8:26716205(Fwd) | downstream_gene_variant; intron_variant; NMD_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs7799652 | chr7:114290483(Fwd) | downstream_gene_variant; intron_variant; NMD_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs7782412 | chr7:114290415(Fwd) | downstream_gene_variant; intron_variant; NMD_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs12505502 | chr4:91568023(Fwd) | downstream_gene_variant; intron_variant; NMD_transcript_variant; upstream_gene_variant | 2 (0/2/0) |
| rs1799913 | chr11:18047255(Fwd) | downstream_gene_variant; intron_variant; NMD_transcript_variant; splice_region_variant; upstream_gene_variant | 1 (0/1/0) |
| rs17055923 | chr8:26611846(Fwd) | downstream_gene_variant; intron_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs10953766 | chr7:114313218(Fwd) | downstream_gene_variant; intron_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs1157690 | chr8:26610152(Fwd) | downstream_gene_variant; intron_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs6592952 | chr7:50560255(Fwd) | downstream_gene_variant; intron_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs9332377 | chr22:19955692(Fwd) | downstream_gene_variant; intron_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs936146 | chr7:114294405(Fwd) | downstream_gene_variant; intron_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs1630498 | chr11:71150785(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/0/1) |
| rs649266 | chr6:16750901(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/0/1) |
| rs3764352 | chr17:37790939(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs930072 | chr5:36666071(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs13306221 | chr11:27722689(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs9676447 | chr19:49424247(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant | 3 (0/2/1) |
| rs2535629 | chr3:52833219(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs1790324 | chr11:71150520(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/0/1) |
| rs3793243 | chr7:73121347(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs736894 | chr11:71152258(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/0/1) |
| rs3817334 | chr11:47650993(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs907094 | chr17:37790371(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs2301064 | chr5:36675699(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs362990 | chr20:10276221(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs2049046 | chr11:27723775(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs17031719 | chr12:102022264(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs362993 | chr20:10276716(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs4869686 | chr5:36679018(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs13270024 | chr8:142201477(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant | 1 (0/1/0) |
| rs2290416 | chr8:144657600(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant; upstream_gene_variant | 1 (0/0/1) |
| rs362998 | chr20:10277621(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant | 3 (1/2/0) |
| rs362986 | chr20:10277034(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant | 1 (0/1/0) |
| rs362987 | chr20:10277452(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant | 5 (1/4/0) |
| rs12690808 | chr7:34606336(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant | 1 (0/1/0) |
| rs12453316 | chr17:71516059(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant | 1 (0/1/0) |
| rs7208257 | chr17:4620497(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (1/0/0) |
| rs7210438 | chr17:79060180(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs11030104 | chr11:27684517(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 2 (1/1/0) |
| rs4075482 | chr17:79074548(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant | 1 (0/1/0) |
| rs2677744 | chr15:91450441(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; upstream_gene_variant | 1 (0/0/1) |
| rs12800438 | chr11:71171003(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant | 1 (0/0/1) |
| rs4697192 | chr4:20851050(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs17520763 | chr4:167839166(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs9322993 | chr14:39605542(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs7103873 | chr11:27700317(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs2046186 | chr8:26711214(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs17520441 | chr4:167809058(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs998850 | chr7:50607388(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs472151 | chr8:26692367(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs6553415 | chr4:167830721(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/1/0) |
| rs10514604 | chr16:84446384(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/0/1) |
| rs2587695 | chr2:120321817(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/0/1) |
| rs8041675 | chr15:37342602(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/0/1) |
| rs1466163 | chr7:50607206(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (1/0/0) |
| rs7103411 | chr11:27700125(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant | 3 (2/1/0) |
| rs8074751 | chr17:63642542(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant | 1 (0/0/1) |
| rs10861968 | chr12:79784553(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs2532274 | chr17:44247164(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs1519480 | chr11:27675712(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs2234689 | chr11:113278483(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs17611827 | chr16:3367061(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs3776568 | chr5:36632611(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs237895 | chr3:8807423(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs6489630 | chr12:5604624(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs878567 | chr5:63255991(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs37022 | chr5:1415629(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 2 (0/2/0) |
| rs1541815 | chr5:36702290(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs10227331 | chr7:157294938(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs6074121 | chr20:10290703(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs1079595 | chr11:113282669(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs3733812 | chr5:36681521(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs2287019 | chr19:46202172(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs3776581 | chr5:36661944(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 2 (0/2/0) |
| rs36684 | chr5:36699827(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs7124601 | chr11:639273(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs607138 | chr6:16749567(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs466630 | chr5:1415404(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs1124491 | chr11:113282090(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 1 (1/0/0) |
| rs13238831 | chr7:128516470(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs2456205 | chr5:52179458(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs1490046 | chr5:173956047(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 1 (0/0/1) |
| rs40358 | chr5:1416142(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 1 (0/1/0) |
| rs1427324 | chr14:59364693(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 2 (0/2/0) |
| rs9534495 | chr13:47429228(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 1 (1/0/0) |