chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97887574478875745TA5GENIChomozygous117380632
97887575478875755GC6GENIChomozygous117380633
97887575978875760GA6GENIChomozygous117380634
97887576178875762CT5GENIChomozygous117380635
97887576678875767CA5GENIChomozygous117380636