chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1157704713157704714TC18GENIChomozygous60909142
1157705875157705876CT20GENIChomozygous60909143
1157707116157707117TTA2GENIChomozygous60909146
1157707514157707515GC14GENIChomozygous60909147
1157707735157707736GGT10GENICheterozygous62233090
1157708632157708633GC12GENIChomozygous60909148