chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97886334678863347AG18GENIChomozygous958673110
97886351778863518TC16GENIChomozygous958673111
97886936678869367AG31GENIChomozygous958673112
97887017378870174AG31GENIChomozygous958673113
97887169478871695TA28GENIChomozygous958673114
97887298178872982CG27GENIChomozygous958673115
97887557078875571TC30GENIChomozygous958673116
97887574478875745TA27GENIChomozygous958673117
97887575478875755GC27GENIChomozygous958673118
97887575978875760GA27GENIChomozygous958673119
97887576178875762CT28GENIChomozygous958673120
97887576678875767CA29GENIChomozygous958673121