chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31565922615659227CT49GENIChomozygous136643510
31565984415659845GA40GENIChomozygous136643511
31566310015663101CA55GENICpossibly homozygous145399655
31566471115664712TG63GENIChomozygous136643512
31566479515664796AG56GENIChomozygous136643513
31566720715667208GA60GENIChomozygous136643514
31566731715667318CT52GENIChomozygous136643515
31566732715667328TC55GENIChomozygous136643516
31566743415667435CT49GENIChomozygous136643517
31566765815667659AG52GENIChomozygous136643518
31566787915667880AG39GENIChomozygous136643519
31566813615668137TC29GENIChomozygous136643520
31566931215669313GA71GENIChomozygous136643522
31566942515669426TA50GENIChomozygous136643523
31566998015669981GC65GENIChomozygous136643524
31567043315670434GA53GENIChomozygous136643525
31567152715671528TG52GENIChomozygous136643526
31567200415672005GA58GENIChomozygous136643527
31567268415672685AG63GENIChomozygous136643528
31567302615673027TG54GENIChomozygous136643529
31567325015673251AG31GENIChomozygous136643530
31567537815675379GA69GENIChomozygous136643531
31567404215674043CA46GENIChomozygous141491717
31566942815669428TTC38GENICpossibly homozygous136549648
31567442915674429AGGG44GENIChomozygous136549649