| rs_ID | Location | Functional Annotation | 
                            
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs7954927 | Chr12:79798573(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs17005561 | Chr12:79800344(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs1465045 | Chr12:79788631(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs11114107 | Chr12:79799216(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs12423434 | Chr12:79801525(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs1245774 | Chr12:79760767(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs17294719 | Chr12:79812271(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs1405495 | Chr12:79799306(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs11114116 | Chr12:79831956(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs1526955 | Chr12:79800028(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs1405497 | Chr12:79804808(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs7295888 | Chr12:79807346(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs4609662 | Chr12:79802176(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs1358243 | Chr12:79803909(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs17041667 | Chr12:79811286(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs7308297 | Chr12:79777844(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs17005588 | Chr12:79809256(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs11612225 | Chr12:79810422(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs11114122 | Chr12:79847040(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs11114088 | Chr12:79794919(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs2400395 | Chr12:79778358(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs7966962 | Chr12:79779417(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs11114112 | Chr12:79812829(Fwd) | intron_variant; nc_transcript_variant; upstream_gene_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs11114027 | Chr12:79775248(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs11113987 | Chr12:79760464(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs11113980 | Chr12:79759364(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs1245765 | Chr12:79777291(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs1245767 | Chr12:79776820(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs1245778 | Chr12:79768171(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs12371960 | Chr12:79778446(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs1245766 | Chr12:79776882(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs1245770 | Chr12:79775359(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs7135647 | Chr12:79839153(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs7315113 | Chr12:79832584(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs9788036 | Chr12:79779307(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs1465051 | Chr12:79778230(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs1465044 | Chr12:79788930(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs10778657 | Chr12:79784735(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs10861976 | Chr12:79794658(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs10861975 | Chr12:79794590(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs10861941 | Chr12:79760388(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs2895728 | Chr12:79802302(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs1465048 | Chr12:79798409(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs1465049 | Chr12:79798494(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs7133421 | Chr12:79798167(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs1465047 | Chr12:79798317(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs1465046 | Chr12:79797095(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs7303658 | Chr12:79797902(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs11608780 | Chr12:79795919(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs11608808 | Chr12:79796144(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs10506815 | Chr12:79793312(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs1405493 | Chr12:79793964(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs4578461 | Chr12:79790779(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs12581451 | Chr12:79791607(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs17005544 | Chr12:79785690(Fwd) | downstream_gene_variant; intron_variant; nc_transcript_variant | 
                                
                            
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs17005546 | Chr12:79790026(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs2701566 | Chr12:79770528(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                        
                                    
                                    
                                    
                                        | rs12579420 | Chr12:79789319(Fwd) | intron_variant; nc_transcript_variant | 
                                
                            
                                
                                
                                    
                                    
                                    
                                        
                                    
                                    
                                        | rs7971881 | Chr12:79781339(Fwd) | feature_truncation; intron_variant; nc_transcript_variant |