chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3112069145112069146CT14GENIChomozygous57991100
3112070291112070337TAGATATAGATATAGATATAGATATAGATATAGATATAGATATAGA----------------------------------------------7GENICheterozygous58619029
3112070400112070420AGATAGATATAGATATAGAG--------------------7GENIChomozygous58619030
3112070525112070526CT5GENIChomozygous57991112
3112071652112071653TC9GENIChomozygous57991115
3112072557112072558TC11GENIChomozygous57991118
3112072945112072946CCAGGAGAAGTG11GENIChomozygous57991121
3112072948112072949CG12GENIChomozygous57991124
3112072950112072952CA--12GENIChomozygous57991127
3112073708112073710AA--9GENIChomozygous57991130
3112074046112074052ACACAC------3GENICheterozygous58690249
3112074298112074299AG12GENIChomozygous57991133
3112075606112075607CCT10GENIChomozygous57991136
3112075623112075624AATT10GENICpossibly homozygous57991139
3112075623112075624AAT10GENICheterozygous58619033
3112076509112076510CCAATAAATA1GENIChomozygous58619034
3112079902112079903GA11GENIChomozygous57991145
3112080993112080994AG10GENIChomozygous57991148
3112083008112083014CACACA------3GENICheterozygous58619036
3112083412112083413TG11GENIChomozygous57991151
3112083477112083478AG14GENIChomozygous57991154
3112083766112083767AT13GENIChomozygous57991157
3112083581112083582AG9GENIChomozygous57603011