chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3112069145112069146CT63GENIChomozygous57991100
3112070398112070402ATAG----19GENICheterozygous57991103
3112070401112070402GGAT20GENICheterozygous57991106
3112070416112070420AGAG----16GENIChomozygous57991109
3112070525112070526CT43GENIChomozygous57991112
3112071652112071653TC37GENIChomozygous57991115
3112072557112072558TC36GENIChomozygous57991118
3112072945112072946CCAGGAGAAGTG17GENIChomozygous57991121
3112072948112072949CG12GENIChomozygous57991124
3112072950112072952CA--11GENIChomozygous57991127
3112073708112073710AA--34GENIChomozygous57991130
3112074298112074299AG37GENIChomozygous57991133
3112075606112075607CCT19GENICpossibly homozygous57991136
3112075623112075624AATT24GENIChomozygous57991139
3112076556112076557CT38GENICheterozygous58389273
3112079435112079436CT57GENICpossibly homozygous57991142
3112079902112079903GA35GENIChomozygous57991145
3112080993112080994AG40GENIChomozygous57991148
3112083412112083413TG38GENIChomozygous57991151
3112083477112083478AG43GENIChomozygous57991154
3112083581112083582AG27GENIChomozygous57603011
3112083766112083767AT44GENIChomozygous57991157