chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3112070525112070526CT14GENICpossibly homozygous57991112
3112071652112071653TC21GENIChomozygous57991115
3112072557112072558TC17GENIChomozygous57991118
3112073708112073710AA--16GENIChomozygous57991130
3112074298112074299AG23GENIChomozygous57991133
3112075623112075624AAT1GENIChomozygous58619033
3112077450112077451A-8GENICheterozygous58321911
3112079902112079903GA15GENICpossibly homozygous57991145
3112079951112079952CT9GENICheterozygous58424411
3112080993112080994AG16GENICpossibly homozygous57991148
3112083412112083413TG19GENICheterozygous57991151
3112083477112083478AG21GENICpossibly homozygous57991154
3112083581112083582AG16GENIChomozygous57603011
3112083766112083767AT30GENICpossibly homozygous57991157