chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95530764855307649GT74GENIChomozygous138598551
95531387455313875CT59GENIChomozygous138598552
95531583355315834GC45GENIChomozygous138598553
95531583455315835TC44GENIChomozygous138598554
95531593155315931A45GENICpossibly homozygous138465162
95531717355317174CT62GENIChomozygous138598555
95531784455317845AG40GENIChomozygous138598556
95531807955318080CA39GENIChomozygous138598557
95531910555319106AC49GENIChomozygous138598558
95531916255319163GA52GENIChomozygous138598559
95532019655320196G48GENIChomozygous138465163
95532043555320435AT36GENIChomozygous138465164
95532244155322442GA50GENIChomozygous138598560
95532487155324872CT45GENIChomozygous138598561
95532585055325851GA38GENIChomozygous138598562
95532604855326050AT42GENICpossibly homozygous138465165
95532746655327467TC32GENIChomozygous138598563
95532758855327589TC34GENIChomozygous138598564
95532799555327996C46GENIChomozygous138465166
95532933355329334AT52GENIChomozygous138598565
95532995255329953CG58GENIChomozygous138598566
95533273855332739GA52GENIChomozygous138598567
95533363855333639AT47GENIChomozygous138598568
95533517255335173TC54GENIChomozygous138598569
95533580755335808TC46GENIChomozygous138598570
95533597655335977TA44GENIChomozygous138598571
95533677955336780AG49GENIChomozygous138598572
95533685355336853A61GENIChomozygous138465167
95533744255337443TC73GENIChomozygous138598573
95533774655337747CG55GENIChomozygous138598574
95533775155337752GC57GENIChomozygous138598575
95533804655338047TC55GENIChomozygous138598576
95532799755327998C47GENICheterozygous148537842
95532799755327998CA47GENIChomozygous154577483