chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X4697896546978966GT13GENIChomozygous977726259
X4697897746978978GA12GENIChomozygous977726260
X4697897846978979AG12GENIChomozygous977726261
X4698531746985318AC15GENIChomozygous977726262
X4700435447004355CT13GENIChomozygous977726263
X4700876747008768AT7GENIChomozygous977726264
X4700983947009840AG25GENIChomozygous977726265
X4701133747011338CA16GENICpossibly homozygous977726266
X4701146647011467AG16GENIChomozygous977726267
X4701155447011555CG26GENIChomozygous977726268
X4701181447011815CT18GENIChomozygous977726269
X4701185047011851AT14GENIChomozygous977726270
X4701271447012715TC15GENIChomozygous977726271
X4701406247014063AG11GENIChomozygous977726272
X4701439547014396TG17GENIChomozygous977726273
X4701486347014864AC8GENIChomozygous977726274
X4701498547014986GC5GENIChomozygous977726275
X4701675447016755TA5GENIChomozygous977726276
X4701877047018771GA10GENIChomozygous977726277
X4702029747020298TC5GENIChomozygous977726278
X4702089747020898AT11GENIChomozygous977726279
X4702126047021261TC15GENIChomozygous977726280
X4702192247021923CT12GENIChomozygous977726281
X4702204547022046GA10GENIChomozygous977726282
X4702295447022955GA13GENIChomozygous977726283
X4702344547023446GC13GENIChomozygous977726284
X4702394447023945GA10GENIChomozygous977726285
X4702589247025893TC12GENIChomozygous977726286