chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122201340722013408GGA1GENIChomozygous50692581
122202288422022885TC1GENIChomozygous50113808
122202288622022887GT1GENIChomozygous50113810
122202291222022913GC12GENIChomozygous50113812
122202298622022987CG3GENICheterozygous50113814
122202307022023071AG2GENIChomozygous50113820
122202307422023075AC2GENIChomozygous50113822
122202308022023081AG3GENIChomozygous50113824
122202313922023140GA20GENICpossibly homozygous50113826
122202316222023163GA8GENICpossibly homozygous50113828
122202316822023169GGAAC4GENICheterozygous50113830
122202319822023199CA5GENICheterozygous50113832
122202322222023223GA1GENIChomozygous50113834