chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109000690990006911TT--2GENICheterozygous51537436
109000748090007481C-9GENIChomozygous51537441
109000895890008959CT20GENICpossibly homozygous51735639
109000932390009324TC8GENICpossibly homozygous51537446
109000972190009722GA18GENICpossibly homozygous51537447
109001068990010690CT13GENICpossibly homozygous51735641