chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3112070525112070526CT9GENIChomozygous57991112
3112071652112071653TC12GENIChomozygous57991115
3112072557112072558TC10GENIChomozygous57991118
3112072950112072952CA--1GENIChomozygous57991127
3112073708112073710AA--10GENIChomozygous57991130
3112074298112074299AG20GENICpossibly homozygous57991133
3112075623112075624AATT4GENICheterozygous57991139
3112075623112075624AAT4GENICheterozygous58619033
3112079902112079903GA16GENICpossibly homozygous57991145
3112080993112080994AG18GENIChomozygous57991148
3112083412112083413TG9GENIChomozygous57991151
3112083477112083478AG11GENICpossibly homozygous57991154
3112083581112083582AG16GENIChomozygous57603011
3112083766112083767AT20GENICpossibly homozygous57991157