chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
176946968869469689AG40GENICpossibly homozygous809807556
176946971669469717GT27GENIChomozygous809807557
176947444769474448TC41GENIChomozygous809807558
176947612869476129TC44GENIChomozygous809807559
176947813969478140AG35GENIChomozygous809807560
176947815569478156AG32GENIChomozygous809807561
176947839969478400TC58GENIChomozygous809807562
176947947169479472CA8GENIChomozygous809807563
176947950569479506CT14GENIChomozygous809807564
176947982069479821CA36GENICheterozygous809807565
176947982169479822CA37GENICheterozygous809807566
176947984269479843AC38GENICheterozygous809807567
176947995869479959AG35GENICheterozygous809807568
176947996869479969TC19GENICheterozygous809807569
176948089369480894TC4GENICheterozygous809807570
176948125969481260GA48GENICheterozygous809807571
176948182969481830TG56GENICheterozygous809807572
176948222069482221AC56GENICheterozygous809807573
176948224069482241CG68GENICheterozygous809807574
176948302669483027GA74GENICheterozygous809807575
176948307669483077CG88GENICheterozygous809807576
176948377669483777AG76GENICheterozygous809807577
176948439469484395GC51GENICheterozygous809807578
176948440969484410GA58GENICheterozygous809807579
176948466069484661TC81GENICheterozygous809807580
176948512269485123AT85GENICheterozygous809807581
176948523769485238AG6GENIChomozygous809807582
176948654669486547AG196GENICheterozygous809807583
176948664469486645AG161GENICheterozygous809807584
176948812469488125AC37GENIChomozygous809807585
176948865369488654TG50GENIChomozygous809807586
176948884469488845CA45GENIChomozygous809807587
176948884869488849AT47GENIChomozygous809807588
176948967769489678AG49GENIChomozygous809807589
176948970169489702GT46GENICpossibly homozygous809807590
176949135269491353AG33GENIChomozygous809807591
176949295269492953GT64GENICheterozygous809807592
176949301669493017TA41GENICheterozygous809807593
176949301769493018CA42GENICheterozygous809807594
176949311569493116GA62GENICpossibly homozygous809807595
176949368969493690GA22GENICpossibly homozygous809807596
176949396869493969CT40GENICpossibly homozygous809807597
176949396969493970CT38GENICpossibly homozygous809807598
176949559169495592CT36GENIChomozygous809807599