chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123963136123963137GT7GENIChomozygous54091558
7123963294123963295AT11GENIChomozygous54091560
7123965962123965963CT26GENICpossibly homozygous54091562
7123966166123966167GA28GENICpossibly homozygous54091564
7123966714123966715AG20GENICpossibly homozygous54091566
7123968071123968072TC20GENIChomozygous54091567
7123968092123968093GA16GENIChomozygous54091569
7123968614123968615CT32GENIChomozygous54091571
7123968675123968676GA19GENICpossibly homozygous54091573
7123969622123969623TC15GENIChomozygous54091575
7123969895123969896CA23GENIChomozygous54091577
7123971180123971181T-2GENIChomozygous54091580
7123972384123972385CT24GENIChomozygous54091582
7123972491123972492AG12GENICpossibly homozygous54091584
7123972517123972518TC11GENIChomozygous54091586
7123972571123972572CT5GENIChomozygous54091587