chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1218351828218351829CT16GENIChomozygous61087736
1218352765218352766CG24GENICpossibly homozygous61087737
1218352839218352840AC10GENIChomozygous61087738
1218353046218353047AC10GENIChomozygous61087739
1218356440218356441AG6GENICheterozygous61087740
1218361723218361724G-11GENICpossibly homozygous61087743