chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1791117779111778GC21GENICheterozygous814139164
1791119109111911AC10GENIChomozygous814139165
1791121599112160AG33GENIChomozygous814139166
1791136519113652GA35GENIChomozygous814139167
1791142129114213AG36GENIChomozygous814139168
1791149469114947AG31GENIChomozygous814139169
1791149569114957AG32GENIChomozygous814139170
1791156009115601CT34GENIChomozygous814139171
1791157259115726TG28GENIChomozygous814139172
1791157919115792GT21GENIChomozygous814139173
1791158519115852GT30GENIChomozygous814139174
1791170459117046CT20GENIChomozygous814139175
1791170669117067AG20GENIChomozygous814139176
1791172069117207CT3GENIChomozygous814139177
1791173049117305AC13GENIChomozygous814139178