chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2189286456189286457TC17GENIChomozygous110171270
2189287963189287964AC19GENIChomozygous110171272
2189289064189289065AT26GENIChomozygous110804974
2189289639189289640AG28GENIChomozygous110171276
2189290740189290741AG32GENIChomozygous110804975
2189290917189290918CT16GENIChomozygous110171278
2189292395189292396CT21GENIChomozygous110804976
2189294378189294379CT29GENIChomozygous110804977
2189294638189294639AG22GENIChomozygous110804978
2189296344189296345GA21GENIChomozygous110804979
2189297131189297131G33GENICpossibly homozygous131298199
2189297602189297603AG25GENIChomozygous110171283
2189298936189298937TC22GENIChomozygous110171287
2189300178189300179CT16GENIChomozygous110804980
2189300522189300523GA32GENIChomozygous110804981
2189301250189301251AG19GENIChomozygous110171293
2189303010189303011CT25GENIChomozygous110804983
2189303134189303135TC29GENIChomozygous110171295
2189303680189303681GC32GENIChomozygous110171296
2189304989189304990CT31GENIChomozygous110804984
2189293265189293265TTG18GENIChomozygous132017818
2189295597189295610CCACCATAGCCAG23GENIChomozygous132017819
2189293268189293269GT18GENIChomozygous120155238