chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1219743849219743850TG9GENIChomozygous108541427
1219744010219744011CT23GENIChomozygous108541428
1219744113219744114AG15GENIChomozygous108541430
1219744721219744722AG12GENIChomozygous108541432
1219745090219745091CA21GENIChomozygous108541434
1219745750219745751GC22GENIChomozygous108541435
1219745822219745823GC11GENIChomozygous108541437
1219745839219745840CT10GENIChomozygous108541439
1219745849219745850TC15GENIChomozygous108541441
1219746826219746827CA18GENICheterozygous108541444
1219746961219746962TA12GENIChomozygous108541446
1219747577219747578CT6GENIChomozygous121179635
1219747945219747946GA23GENIChomozygous108541448
1219747998219747999TC18GENIChomozygous108541449
1219748059219748060CA4GENIChomozygous120512247
1219748716219748717TC13GENIChomozygous108541453
1219749885219749886GA13GENIChomozygous108541454
1219750513219750514CT16GENIChomozygous108541456
1219751452219751453GA29GENIChomozygous108541460
1219752711219752712GT9GENIChomozygous108541464
1219752747219752748CA6GENIChomozygous108541466
1219755646219755647CT8GENIChomozygous108541468
1219756028219756029AG21GENIChomozygous108541470
1219756761219756762CT17GENIChomozygous108541472
1219757194219757195AC12GENIChomozygous108541474