chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104528344145283442GT77GENIChomozygous51636177
104528729545287296TA51GENIChomozygous51636178
104528759245287594AC--8GENIChomozygous51442167
104528762145287632CACACACACAC-----------19GENICpossibly homozygous51636179
104528875445288756AC--56GENIChomozygous51636180
104528982445289825GGC15GENICpossibly homozygous51442169
104528983545289836T-16GENICheterozygous51442170