chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
53349845533498456AG59GENIChomozygous137420659
53349972833499729C16GENIChomozygous403137660
53349972833499729CT16GENICheterozygous403137661
53350409833504099CT47GENIChomozygous137420661
53350515933505160CT42GENIChomozygous137420662
53350524333505244GA36GENIChomozygous137420663
53350524433505245AG37GENIChomozygous137420664
53350525133505252TA35GENIChomozygous137420665
53350527833505279GA39GENIChomozygous137420666
53350529133505292GC40GENIChomozygous137420667
53350532133505322TC43GENIChomozygous137420668
53350532633505327TC44GENIChomozygous137420669
53350579133505792GA48GENIChomozygous137420670
53350597833505979TC53GENIChomozygous137420671
53350920633509207AG46GENIChomozygous137420673
53351163533511636AG55GENIChomozygous137420676
53351198933511990CG42GENIChomozygous137420677
53350779033507791GA61GENIChomozygous144719884
53350360733503612CTCTA30GENIChomozygous137299340
53350522033505220G37GENIChomozygous137299341
53350907633509077GC37GENIChomozygous144719885
53350999233509993GT23GENIChomozygous144719886
53350999933510000CT22GENIChomozygous144719887
53351527833515279AG42GENIChomozygous137420680
53351640733516408GA53GENIChomozygous137420682
53351658233516583AG37GENICpossibly homozygous144719888
53351764333517644TC52GENIChomozygous137420684
53351834033518341TC49GENIChomozygous137420686
53351841533518416GA45GENIChomozygous144719889
53351841633518417AC45GENIChomozygous144719890
53351852533518526CT51GENIChomozygous137420687
53351857433518575GT48GENIChomozygous144719891
53351857633518577TA48GENIChomozygous144719892
53351857733518578GC48GENIChomozygous144719893
53351860533518606CT50GENIChomozygous137420688
53351548533515485T43GENICpossibly homozygous144696671
53351658433516587AAG35GENIChomozygous144696672