chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3112069145112069146CT70GENIChomozygous57991100
3112070398112070402ATAG----19GENICheterozygous57991103
3112070401112070402GGAT19GENICheterozygous57991106
3112070416112070420AGAG----22GENIChomozygous57991109
3112070525112070526CT61GENIChomozygous57991112
3112071652112071653TC66GENIChomozygous57991115
3112072557112072558TC68GENIChomozygous57991118
3112072945112072946CCAGGAGAAGTG29GENIChomozygous57991121
3112072948112072949CG21GENIChomozygous57991124
3112072950112072952CA--18GENIChomozygous57991127
3112073708112073710AA--60GENIChomozygous57991130
3112074298112074299AG56GENIChomozygous57991133
3112075606112075607CCT25GENICpossibly homozygous57991136
3112075623112075624AATT22GENIChomozygous57991139
3112079435112079436CT45GENICpossibly homozygous57991142
3112079902112079903GA46GENIChomozygous57991145
3112080993112080994AG52GENIChomozygous57991148
3112083412112083413TG55GENIChomozygous57991151
3112083477112083478AG64GENIChomozygous57991154
3112083766112083767AT46GENIChomozygous57991157
3112083581112083582AG73GENIChomozygous57603011