chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7129728957129728958CT7GENIChomozygous54109510
7129729266129729267TG20GENICpossibly homozygous54109511
7129730321129730322TG18GENICpossibly homozygous54109512
7129730958129730959CT13GENICpossibly homozygous54109513
7129732151129732152TC26GENICpossibly homozygous54109514
7129732295129732296GA25GENICpossibly homozygous54109515
7129732470129732471CT21GENICpossibly homozygous54109516
7129732578129732579CA13GENIChomozygous54109517
7129738615129738616CT16GENIChomozygous54109519