chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123963136123963137GT41GENIChomozygous54091558
7123963294123963295AT39GENIChomozygous54091560
7123965962123965963CT24GENIChomozygous54091562
7123966166123966167GA39GENIChomozygous54091564
7123966714123966715AG26GENIChomozygous54091566
7123968071123968072TC19GENIChomozygous54091567
7123968092123968093GA15GENIChomozygous54091569
7123968614123968615CT30GENIChomozygous54091571
7123968675123968676GA33GENIChomozygous54091573
7123969622123969623TC34GENIChomozygous54091575
7123969895123969896CA30GENIChomozygous54091577
7123971036123971038AT--33GENIChomozygous54091578
7123971180123971181T-23GENICpossibly homozygous54091580
7123972384123972385CT23GENIChomozygous54091582
7123972491123972492AG5GENIChomozygous54091584
7123972517123972518TC19GENIChomozygous54091586
7123972571123972572CT15GENIChomozygous54091587