rs_ID |
Location |
Functional Annotation |
rs9991390 |
chr4:167824208(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs4241628 |
chr4:167796003(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7693556 |
chr4:168142640(Fwd) |
intron_variant; NMD_transcript_variant |
rs10020340 |
chr4:167824350(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10027880 |
chr4:167798911(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs9997969 |
chr4:167826468(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10517907 |
chr4:167814606(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10018856 |
chr4:167828755(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs3936140 |
chr4:167825025(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10019607 |
chr4:167821252(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7689694 |
chr4:167661368(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs954722 |
chr4:167744429(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10022395 |
chr4:167821848(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7678556 |
chr4:167661512(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10517910 |
chr4:167796914(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs12649447 |
chr4:167822014(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10021354 |
chr4:167654427(Fwd) |
downstream_gene_variant |
rs17702127 |
chr4:167799695(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10019784 |
chr4:167823715(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7681289 |
chr4:167659338(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10001800 |
chr4:167812963(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17598884 |
chr4:167815236(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2124450 |
chr4:167665046(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs6553313 |
chr4:167815850(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17520623 |
chr4:167815902(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2198736 |
chr4:167671562(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs6553317 |
chr4:167816249(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10014429 |
chr4:167816775(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2219236 |
chr4:167664510(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7679810 |
chr4:167816602(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10014713 |
chr4:167816995(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2318485 |
chr4:167664591(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10011960 |
chr4:167743180(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17520406 |
chr4:167802961(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs12715959 |
chr4:167674678(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs921856 |
chr4:167745216(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10012697 |
chr4:167806056(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2219238 |
chr4:167696538(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2318494 |
chr4:167752224(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs4314314 |
chr4:167813744(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2124456 |
chr4:167691100(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs6552659 |
chr4:167755348(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17520532 |
chr4:167813818(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10003311 |
chr4:167670960(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs6552687 |
chr4:167757806(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2124457 |
chr4:167683728(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs745244 |
chr4:167694843(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7698457 |
chr4:167699942(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7693792 |
chr4:167661037(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs952650 |
chr4:167658259(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17052594 |
chr4:167698563(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7698841 |
chr4:167700120(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs11940325 |
chr4:167671168(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs4860020 |
chr4:167691805(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs4627894 |
chr4:167691711(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs4860018 |
chr4:167691688(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs4859978 |
chr4:167691609(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10003506 |
chr4:167834179(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs6844855 |
chr4:167694753(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10031083 |
chr4:167830128(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2318489 |
chr4:167694585(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10013298 |
chr4:167765792(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs4860022 |
chr4:167693875(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs9999386 |
chr4:167834440(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs4859980 |
chr4:167691950(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17598718 |
chr4:167802722(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7661721 |
chr4:167809874(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17598700 |
chr4:167802246(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs11132570 |
chr4:167808432(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17520371 |
chr4:167801983(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs6826435 |
chr4:167802839(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs9997140 |
chr4:167801478(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs13123001 |
chr4:167799899(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs9996973 |
chr4:167801275(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs5028425 |
chr4:167809133(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs9996631 |
chr4:167800916(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs4128681 |
chr4:167796603(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10021984 |
chr4:167799598(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10517908 |
chr4:167817905(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs9990732 |
chr4:167799451(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs4860003 |
chr4:167815372(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10049559 |
chr4:167787309(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10029969 |
chr4:167781482(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10009507 |
chr4:168016038(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs12331675 |
chr4:167773860(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs12648509 |
chr4:167781906(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17520051 |
chr4:167739119(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs6823089 |
chr4:167735135(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs13103887 |
chr4:167794933(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17053125 |
chr4:168160774(Fwd) |
upstream_gene_variant |
rs10032567 |
chr4:167732948(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7672200 |
chr4:167790958(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs6553015 |
chr4:167788342(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2010146 |
chr4:167917926(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs1896481 |
chr4:167908657(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs1016341 |
chr4:167738606(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs13127151 |
chr4:167685013(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs12501132 |
chr4:167685139(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7689431 |
chr4:167685199(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10024474 |
chr4:167689996(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2054145 |
chr4:167684049(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2054144 |
chr4:167684182(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2318488 |
chr4:167684898(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs13143115 |
chr4:167684981(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10517901 |
chr4:167674905(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2305593 |
chr4:167675635(Fwd) |
3_prime_UTR_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2168405 |
chr4:167683661(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2054146 |
chr4:167683902(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7674160 |
chr4:167655602(Fwd) |
3_prime_UTR_variant; downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant |
rs7695294 |
chr4:167655803(Fwd) |
3_prime_UTR_variant; downstream_gene_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant |
rs7691894 |
chr4:167663664(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2219234 |
chr4:167671875(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs6826647 |
chr4:167652162(Fwd) |
downstream_gene_variant |
rs7658860 |
chr4:167651397(Fwd) |
downstream_gene_variant |
rs3762244 |
chr4:167655482(Fwd) |
3_prime_UTR_variant; downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant |
rs977643 |
chr4:167653371(Fwd) |
downstream_gene_variant |
rs2168402 |
chr4:167765735(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7698485 |
chr4:167760175(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs6845116 |
chr4:167753071(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7658503 |
chr4:167651241(Fwd) |
downstream_gene_variant |
rs6819071 |
chr4:167650690(Fwd) |
downstream_gene_variant |
rs7669089 |
chr4:167753460(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs6834387 |
chr4:167771434(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2077684 |
chr4:167920238(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs12498755 |
chr4:168055022(Fwd) |
intron_variant; NMD_transcript_variant |
rs13120774 |
chr4:168114993(Fwd) |
intron_variant; NMD_transcript_variant |
rs13125499 |
chr4:167945718(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs815225 |
chr4:168073690(Fwd) |
intron_variant; NMD_transcript_variant |
rs13137584 |
chr4:167921800(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs6553573 |
chr4:168069787(Fwd) |
intron_variant; NMD_transcript_variant |
rs10010502 |
chr4:167976180(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17052929 |
chr4:167975079(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs815222 |
chr4:168074573(Fwd) |
intron_variant; NMD_transcript_variant |
rs1896480 |
chr4:167899528(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs1564862 |
chr4:168070938(Fwd) |
intron_variant; NMD_transcript_variant |
rs815237 |
chr4:168056563(Fwd) |
intron_variant; NMD_transcript_variant |
rs2059735 |
chr4:167920518(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs815233 |
chr4:168063002(Fwd) |
intron_variant; NMD_transcript_variant |
rs13117854 |
chr4:167920443(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs1579404 |
chr4:168029135(Fwd) |
intron_variant; NMD_transcript_variant |
rs2220190 |
chr4:168086766(Fwd) |
intron_variant; NMD_transcript_variant |
rs2629387 |
chr4:168033949(Fwd) |
intron_variant; NMD_transcript_variant |
rs13137059 |
chr4:168083435(Fwd) |
intron_variant; NMD_transcript_variant |
rs11132867 |
chr4:168027788(Fwd) |
intron_variant; NMD_transcript_variant; upstream_gene_variant |
rs13139648 |
chr4:168106348(Fwd) |
intron_variant; NMD_transcript_variant |
rs860092 |
chr4:168055580(Fwd) |
intron_variant; NMD_transcript_variant |
rs13109419 |
chr4:168098184(Fwd) |
intron_variant; NMD_transcript_variant |
rs815213 |
chr4:168034257(Fwd) |
intron_variant; NMD_transcript_variant |
rs13124945 |
chr4:168016382(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs13110285 |
chr4:168000626(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7680101 |
chr4:168082736(Fwd) |
intron_variant; NMD_transcript_variant |
rs11939479 |
chr4:168022694(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17599890 |
chr4:168047238(Fwd) |
intron_variant; NMD_transcript_variant |
rs4634252 |
chr4:167862936(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17599192 |
chr4:167891387(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17521233 |
chr4:167962200(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10517919 |
chr4:167962448(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17599698 |
chr4:167998392(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17599814 |
chr4:168034319(Fwd) |
intron_variant; NMD_transcript_variant |
rs17519766 |
chr4:167696109(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs1057377 |
chr4:167656073(Fwd) |
3_prime_UTR_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; stop_retained_variant |
rs17519333 |
chr4:167653444(Fwd) |
downstream_gene_variant |
rs11935662 |
chr4:167697937(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs35646569 |
chr4:167778165(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs6828808 |
chr4:167853560(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2318484 |
chr4:167662287(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7670065 |
chr4:167709990(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10517903 |
chr4:167711854(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10517906 |
chr4:167809560(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs1037630 |
chr4:167692474(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2318486 |
chr4:167683517(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17519417 |
chr4:167659185(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7678726 |
chr4:167661584(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs6552223 |
chr4:167694282(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs3925714 |
chr4:167692553(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17052606 |
chr4:167716288(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10009425 |
chr4:167736917(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17052635 |
chr4:167736380(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs1023875 |
chr4:167738944(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10032215 |
chr4:167730244(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs1551490 |
chr4:167727651(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs6834977 |
chr4:167735652(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10517927 |
chr4:168147524(Fwd) |
intron_variant; NMD_transcript_variant |
rs10034594 |
chr4:167730577(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17703512 |
chr4:168137719(Fwd) |
intron_variant; NMD_transcript_variant |
rs17600510 |
chr4:168156453(Fwd) |
upstream_gene_variant |
rs7435823 |
chr4:168044726(Fwd) |
intron_variant; NMD_transcript_variant |
rs7695680 |
chr4:167954844(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7677172 |
chr4:167954983(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs1427623 |
chr4:167953101(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs1427624 |
chr4:167953146(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs12511389 |
chr4:167886956(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7662976 |
chr4:167951933(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs9284943 |
chr4:167952824(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10471190 |
chr4:167950682(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs13124292 |
chr4:167951139(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs1365944 |
chr4:167945766(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7671612 |
chr4:167945914(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7685624 |
chr4:167943152(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7664643 |
chr4:167944755(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2703842 |
chr4:167938604(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs12643432 |
chr4:167939925(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2558138 |
chr4:167922567(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs6553490 |
chr4:167933010(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs6553431 |
chr4:167857723(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs4992204 |
chr4:168015230(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs6818745 |
chr4:167956606(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs12505847 |
chr4:168013069(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17646122 |
chr4:167925272(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs1427626 |
chr4:167987504(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs13137632 |
chr4:167982046(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs1344657 |
chr4:167947544(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs9968512 |
chr4:168052023(Fwd) |
intron_variant; NMD_transcript_variant |
rs13125626 |
chr4:168052793(Fwd) |
intron_variant; NMD_transcript_variant |
rs13123137 |
chr4:167939694(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10517917 |
chr4:168039224(Fwd) |
intron_variant; NMD_transcript_variant |
rs6848156 |
chr4:167924264(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10471192 |
chr4:167952801(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7688165 |
chr4:168008751(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10006554 |
chr4:167972084(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17052788 |
chr4:167951728(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7666534 |
chr4:168006019(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs12498852 |
chr4:167960855(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10517922 |
chr4:167918667(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs11132847 |
chr4:167959102(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs12509015 |
chr4:167916803(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs11132846 |
chr4:167958698(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10517920 |
chr4:167932509(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10008797 |
chr4:168075537(Fwd) |
intron_variant; NMD_transcript_variant |
rs13113307 |
chr4:167958068(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2873821 |
chr4:167919134(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7659299 |
chr4:168054033(Fwd) |
intron_variant; NMD_transcript_variant |
rs6854001 |
chr4:167956817(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17052698 |
chr4:167893984(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs11931152 |
chr4:167956473(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7662556 |
chr4:167891502(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs765749 |
chr4:167955753(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17052724 |
chr4:167912423(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7668212 |
chr4:167955098(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs6823223 |
chr4:167907187(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs6829378 |
chr4:167995689(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10014833 |
chr4:167847262(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs9312449 |
chr4:167850192(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10461314 |
chr4:167850572(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2198743 |
chr4:167738464(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17645671 |
chr4:167802803(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs4444855 |
chr4:167830032(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs8180142 |
chr4:167844096(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant |
rs4416504 |
chr4:167841057(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant |
rs10020692 |
chr4:167843608(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant |
rs1037629 |
chr4:167738195(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs12331021 |
chr4:168032755(Fwd) |
intron_variant; NMD_transcript_variant |
rs1365949 |
chr4:168004991(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10050205 |
chr4:167992004(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10023610 |
chr4:167976092(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7682844 |
chr4:167867095(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7682265 |
chr4:167866843(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs13106418 |
chr4:167900115(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10005354 |
chr4:167869220(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2703843 |
chr4:167916904(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2703840 |
chr4:167903493(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10006283 |
chr4:167971872(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs11132844 |
chr4:167958392(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7697703 |
chr4:168016229(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2114756 |
chr4:168020480(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs6851188 |
chr4:167857369(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs9998279 |
chr4:168002419(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs12649043 |
chr4:167861017(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs7671983 |
chr4:168012450(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs11943574 |
chr4:167876114(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs13144616 |
chr4:167865711(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs4241629 |
chr4:167877987(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs6823924 |
chr4:167866712(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs11935140 |
chr4:167887940(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10028687 |
chr4:167862345(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs4431249 |
chr4:167888779(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17052681 |
chr4:167864383(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs12019279 |
chr4:167889938(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs13434541 |
chr4:168002014(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2558133 |
chr4:167908246(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17645839 |
chr4:167837678(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2703841 |
chr4:167907991(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2059734 |
chr4:167911815(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs1346379 |
chr4:167910216(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs1863782 |
chr4:167914437(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2703844 |
chr4:167913404(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs728112 |
chr4:167917532(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2558135 |
chr4:167916274(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs4860001 |
chr4:167815322(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs13101560 |
chr4:167894298(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2558146 |
chr4:167894030(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10026895 |
chr4:167791824(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs13138354 |
chr4:167897360(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs4241627 |
chr4:167724598(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs1896478 |
chr4:167894912(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs1896479 |
chr4:167899470(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs6849616 |
chr4:167750625(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs10000535 |
chr4:167898317(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs1427630 |
chr4:167905722(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2198744 |
chr4:167713699(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs1863783 |
chr4:167901422(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs17701990 |
chr4:167749783(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |