chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122834070528340706CCTTTATT9GENIChomozygous50158568
122834070828340709CCAT8GENIChomozygous50158570
122834385128343852GT18GENICheterozygous50375359
122834526328345264TTC8GENICheterozygous50304984
122834385528343856GT17GENICheterozygous50407491
122834526328345264TTCC8GENICpossibly homozygous50407493