chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X4697896546978966GT15GENIChomozygous999096109
X4697897746978978GA18GENIChomozygous999096110
X4697897846978979AG18GENIChomozygous999096111
X4698531746985318AC9GENIChomozygous999096112
X4700435447004355CT10GENIChomozygous999096113
X4700460947004610TC12GENIChomozygous999096114
X4700876747008768AT10GENIChomozygous999096115
X4700983947009840AG14GENIChomozygous999096116
X4701133747011338CA13GENICpossibly homozygous999096117
X4701146647011467AG12GENIChomozygous999096118
X4701155447011555CG18GENIChomozygous999096119
X4701181447011815CT19GENIChomozygous999096120
X4701185047011851AT16GENIChomozygous999096121
X4701271447012715TC13GENIChomozygous999096122
X4701406247014063AG17GENIChomozygous999096123
X4701439547014396TG10GENIChomozygous999096124
X4701498547014986GC13GENIChomozygous999096125
X4701660847016609AG7GENIChomozygous999096126
X4701675447016755TA9GENIChomozygous999096127
X4701877047018771GA11GENIChomozygous999096128
X4702089747020898AT10GENIChomozygous999096129
X4702126047021261TC13GENIChomozygous999096130
X4702192247021923CT7GENIChomozygous999096131
X4702204547022046GA21GENIChomozygous999096132
X4702295447022955GA12GENIChomozygous999096133
X4702344547023446GC11GENIChomozygous999096134
X4702394447023945GA11GENIChomozygous999096135
X4702589247025893TC12GENIChomozygous999096136