chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3112069145112069146CT22GENIChomozygous57991100
3112070398112070402ATAG----9GENIChomozygous57991103
3112070401112070402GGAT9GENIChomozygous57991106
3112070416112070420AGAG----13GENIChomozygous57991109
3112070525112070526CT27GENIChomozygous57991112
3112071652112071653TC35GENIChomozygous57991115
3112072557112072558TC27GENIChomozygous57991118
3112072945112072946CCAGGAGAAGTG19GENIChomozygous57991121
3112072948112072949CG11GENIChomozygous57991124
3112072950112072952CA--10GENIChomozygous57991127
3112073708112073710AA--37GENIChomozygous57991130
3112074298112074299AG23GENIChomozygous57991133
3112075606112075607CCT9GENICpossibly homozygous57991136
3112075623112075624AATT14GENIChomozygous57991139
3112079435112079436CT28GENICheterozygous57991142
3112079902112079903GA10GENIChomozygous57991145
3112080993112080994AG22GENIChomozygous57991148
3112083412112083413TG26GENIChomozygous57991151
3112083477112083478AG28GENIChomozygous57991154
3112083766112083767AT21GENIChomozygous57991157
3112083581112083582AG36GENIChomozygous57603011