chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97887574478875745TA17GENIChomozygous929749865
97887575478875755GC17GENIChomozygous929749866
97887575978875760GA18GENIChomozygous929749867
97887576178875762CT18GENIChomozygous929749868
97887576678875767CA18GENIChomozygous929749869