chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97886624278866242A33GENIChomozygous128726712
97886828878868289C18GENICheterozygous130773421
97887574478875745TA18GENIChomozygous117594020
97887575478875755GC16GENIChomozygous117594022
97887575978875760GA15GENIChomozygous117594024
97887576178875762CT15GENIChomozygous117594026
97887576678875767CA14GENIChomozygous117594028