chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3112335188112335189GA54GENIChomozygous111675574
3112340342112340342G54GENIChomozygous127919117
3112341054112341055GA57GENIChomozygous111675575
3112341687112341688CT55GENIChomozygous111675576
3112342273112342273G53GENIChomozygous127919118
3112342283112342283T53GENIChomozygous127919119
3112343205112343206AG58GENIChomozygous111675577
3112344576112344577G9GENIChomozygous132459069
3112344588112344589G9GENIChomozygous132459070
3112346136112346137AG61GENIChomozygous111675579
3112347993112347994GA68GENIChomozygous111675580
3112350880112350881AG50GENIChomozygous111675581
3112352588112352589AG74GENIChomozygous111675582
3112353110112353111T55GENIChomozygous133115601
3112353112112353115GAT55GENIChomozygous133115602
3112353395112353396AC49GENIChomozygous111675584
3112353741112353749TATATATG42GENIChomozygous132459071
3112353794112353795AG30GENICheterozygous121853888
3112353796112353797AG30GENICheterozygous112006841
3112354013112354014AT46GENIChomozygous112139359
3112354162112354162C60GENIChomozygous127919120
3112355711112355711T49GENIChomozygous127919121
3112355718112355718T49GENIChomozygous127919122
3112355741112355742GA52GENIChomozygous111675586
3112355767112355768A50GENIChomozygous127919123
3112355772112355772G53GENIChomozygous127919124
3112356311112356313TC17GENICheterozygous127919125
3112356314112356317CTC18GENICheterozygous127919126
3112362192112362199GGAAAGC45GENIChomozygous127919127
3112362375112362376AG58GENIChomozygous111675590