chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214178917214178918GA19GENICpossibly homozygous62099421
1214180025214180026AC6GENIChomozygous61079796
1214180082214180083CG12GENIChomozygous61079797
1214180539214180540CA20GENICpossibly homozygous61079798
1214180752214180753CT19GENIChomozygous61079799
1214181151214181152T-11GENIChomozygous61079800
1214181352214181353AT1GENIChomozygous61079805
1214181357214181358AT1GENIChomozygous61079806
1214181360214181361AG1GENIChomozygous61079807
1214181361214181362AG1GENIChomozygous61079808
1214181363214181364AG1GENIChomozygous61079809
1214181391214181392AG10GENIChomozygous61079810
1214181548214181549CT3GENICheterozygous61079811
1214181752214181753TC13GENICheterozygous61079813