chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121235910712359108CT14GENICpossibly homozygous668725502
121235937512359382CTGCAAT-------3GENIChomozygous768233551
121236092912360930TC16GENICpossibly homozygous668725503
121236100612361007CT17GENIChomozygous668725504
121236109412361095CT8GENIChomozygous668725505
121236159912361600TC22GENIChomozygous668725506
121236161812361619TC17GENIChomozygous668725507
121236167812361679TC15GENICpossibly homozygous668725508
121236171912361720GGTTGT5GENICheterozygous768233552