chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97886624278866242A15GENIChomozygous128726712
97886828878868289C10GENICheterozygous130773421
97887574478875745TA29GENIChomozygous117594020
97887575478875755GC26GENIChomozygous117594022
97887575978875760GA24GENIChomozygous117594024
97887576178875762CT24GENIChomozygous117594026
97887576678875767CA23GENIChomozygous117594028