chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96231889162318892TC44GENIChomozygous142155103
96232011362320113TG45GENIChomozygous142114759
96232135062321350G43GENIChomozygous142114760
96232143462321435GT46GENIChomozygous142155105
96232294362322944TC51GENIChomozygous142155110
96232324262323243AG76GENIChomozygous142155112
96232360162323602GA62GENIChomozygous147286290
96232365762323658AG68GENIChomozygous147286291
96232367262323673TC63GENIChomozygous147286292
96232381462323815CT68GENIChomozygous147286293
96232385662323857CA63GENIChomozygous147286294
96232385962323860TC66GENIChomozygous147286295
96232412262324123AG56GENIChomozygous147286296
96232421262324213CA43GENIChomozygous147286297
96232456562324566CA72GENIChomozygous147286298
96232539362325394GA49GENIChomozygous147286299
96232590762325907T45GENICpossibly homozygous147283452