chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97886624278866242A31GENIChomozygous128726712
97887574478875745TA23GENIChomozygous117594020
97887575478875755GC23GENIChomozygous117594022
97887575978875760GA23GENIChomozygous117594024
97887576178875762CT21GENIChomozygous117594026
97887576678875767CA22GENIChomozygous117594028