chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
53349845533498456AG40GENIChomozygous137420659
53349972833499729C35GENIChomozygous403137660
53349972833499729CT35GENICheterozygous403137661
53350001533500016AG51GENIChomozygous137420660
53350322533503226TA41GENICpossibly homozygous143212545
53350409833504099CT49GENIChomozygous137420661
53350515933505160CT39GENIChomozygous137420662
53350524333505244GA36GENIChomozygous137420663
53350524433505245AG37GENIChomozygous137420664
53350525133505252TA32GENIChomozygous137420665
53350527833505279GA28GENIChomozygous137420666
53350529133505292GC29GENIChomozygous137420667
53350532133505322TC38GENIChomozygous137420668
53350532633505327TC39GENIChomozygous137420669
53350579133505792GA50GENIChomozygous137420670
53350597833505979TC51GENIChomozygous137420671
53350875733508758TA45GENICpossibly homozygous137420672
53350920633509207AG49GENIChomozygous137420673
53350938033509381TC61GENIChomozygous137420674
53350940733509408CT62GENICpossibly homozygous137420675
53351163533511636AG62GENIChomozygous137420676
53351198933511990CG43GENIChomozygous137420677
53351291733512918TA45GENIChomozygous137420678
53350360733503612CTCTA33GENIChomozygous137299340
53350522033505220G39GENIChomozygous137299341
53350716133507161TA51GENICpossibly homozygous137299342
53350909033509091T45GENIChomozygous137299343
53350941833509418TG64GENICpossibly homozygous137299344
53351302033513021AG36GENIChomozygous137420679
53351527833515279AG35GENIChomozygous137420680
53351611133516112AG60GENIChomozygous137420681
53351640733516408GA52GENIChomozygous137420682
53351729033517291T38GENIChomozygous137299345
53351760233517603GT55GENICpossibly homozygous137420683
53351764333517644TC51GENIChomozygous137420684
53351788633517887AG60GENIChomozygous137420685
53351834033518341TC41GENIChomozygous137420686
53351852533518526CT57GENIChomozygous137420687
53351860533518606CT62GENIChomozygous137420688
53351867833518678A56GENIChomozygous137299346