chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
53349845533498456AG28GENIChomozygous137420659
53349972833499729C11GENIChomozygous403137660
53349972833499729CT11GENICheterozygous403137661
53350001533500016AG25GENIChomozygous137420660
53350409833504099CT12GENIChomozygous137420661
53350515933505160CT14GENIChomozygous137420662
53350524333505244GA19GENIChomozygous137420663
53350524433505245AG19GENIChomozygous137420664
53350525133505252TA18GENIChomozygous137420665
53350527833505279GA15GENIChomozygous137420666
53350529133505292GC12GENIChomozygous137420667
53350532133505322TC16GENIChomozygous137420668
53350532633505327TC17GENIChomozygous137420669
53350579133505792GA17GENIChomozygous137420670
53350597833505979TC19GENIChomozygous137420671
53350875733508758TA19GENIChomozygous137420672
53350920633509207AG24GENIChomozygous137420673
53350938033509381TC21GENIChomozygous137420674
53350940733509408CT21GENIChomozygous137420675
53350360733503612CTCTA14GENIChomozygous137299340
53350522033505220G17GENIChomozygous137299341
53350716133507161TA12GENIChomozygous137299342
53350909033509091T14GENIChomozygous137299343
53350941833509418TG24GENIChomozygous137299344
53351302033513021AG17GENIChomozygous137420679
53351163533511636AG25GENIChomozygous137420676
53351198933511990CG20GENIChomozygous137420677
53351291733512918TA25GENIChomozygous137420678
53351527833515279AG17GENIChomozygous137420680
53351611133516112AG25GENIChomozygous137420681
53351640733516408GA26GENIChomozygous137420682
53351729033517291T17GENIChomozygous137299345
53351760233517603GT19GENIChomozygous137420683
53351764333517644TC22GENIChomozygous137420684
53351788633517887AG18GENICpossibly homozygous137420685
53351834033518341TC16GENIChomozygous137420686
53351852533518526CT30GENIChomozygous137420687
53351860533518606CT25GENIChomozygous137420688
53351867833518678A18GENIChomozygous137299346