chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122202288422022885TC6GENIChomozygous50113808
122202288622022887GT7GENIChomozygous50113810
122202291222022913GC14GENIChomozygous50113812
122202298622022987CG3GENIChomozygous50113814
122202303222023033TG1GENIChomozygous50113816
122202307022023071AG3GENIChomozygous50113820
122202307422023075AC4GENIChomozygous50113822
122202308022023081AG4GENIChomozygous50113824
122202313922023140GA13GENICheterozygous50113826
122202316222023163GA3GENIChomozygous50113828
122202316822023169GGAAC2GENIChomozygous50113830
122202319822023199CA6GENIChomozygous50113832
122202322222023223GA3GENIChomozygous50113834