chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221068683221068684GC20GENIChomozygous61093615
1221069421221069422TC17GENIChomozygous61093617
1221069528221069529GA14GENIChomozygous61093618
1221072012221072013CT30GENIChomozygous61093619
1221074274221074275GT20GENIChomozygous61093620
1221076014221076015AC21GENIChomozygous61093621
1221076373221076376AAG---10GENIChomozygous61093622
1221076652221076653TTAA9GENIChomozygous61093623
1221077964221077982ACACACACACACACACAC------------------9GENICheterozygous62200041
1221077966221077982ACACACACACACACAC----------------9GENICheterozygous62236974
1221077968221077982ACACACACACACAC--------------9GENICheterozygous62200043
1221079359221079360CCT6GENIChomozygous61093625
1221080275221080276AC20GENIChomozygous61093628