chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7129728957129728958CT2GENIChomozygous54109510
7129729266129729267TG8GENIChomozygous54109511
7129730321129730322TG12GENIChomozygous54109512
7129730958129730959CT21GENIChomozygous54109513
7129732151129732152TC14GENIChomozygous54109514
7129732295129732296GA21GENIChomozygous54109515
7129732470129732471CT26GENIChomozygous54109516
7129732578129732579CA17GENIChomozygous54109517
7129733368129733370AA--16GENICpossibly homozygous54241211
7129733369129733370A-16GENICheterozygous54109518
7129738615129738616CT12GENIChomozygous54109519