chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1797783169778316A10GENIChomozygous131750615
1797800849780085GT24GENIChomozygous111230206
1797808899780890AG22GENIChomozygous110953099
1797810219781022CG18GENIChomozygous110953101
1797817429781743CA15GENICpossibly homozygous111230208
1797803379780338AC19GENIChomozygous111166990
1797828489782849AG24GENIChomozygous110953117
1797837369783737G16GENIChomozygous129421296
1797841539784154GT17GENIChomozygous111230212
1797863459786346GT22GENIChomozygous111230214
1797866129786613TC18GENIChomozygous110953119
1797873699787370AG20GENIChomozygous110953123
1797894839789484CT16GENIChomozygous111230216
1797911739791174GA33GENIChomozygous111230218
1797914929791493CT28GENIChomozygous111230221