chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1797783169778316A22GENICpossibly homozygous131750615
1797800849780085GT29GENICpossibly homozygous111230206
1797808899780890AG52GENIChomozygous110953099
1797810219781022CG54GENIChomozygous110953101
1797817429781743CA46GENICpossibly homozygous111230208
1797828489782849AG38GENIChomozygous110953117
1797837369783737G35GENIChomozygous129421296
1797841539784154GT50GENIChomozygous111230212
1797863459786346GT37GENIChomozygous111230214
1797866129786613TC34GENIChomozygous110953119
1797873699787370AG34GENIChomozygous110953123
1797894839789484CT52GENIChomozygous111230216
1797803379780338AC39GENIChomozygous111166990
1797911739791174GA57GENIChomozygous111230218
1797914929791493CT61GENIChomozygous111230221