chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3147506046147506052GCTGCT------2GENIChomozygous58561950
3147506436147506437CG30GENICpossibly homozygous58224920
3147507467147507468CG13GENIChomozygous57727518
3147507761147507762CCTT2GENIChomozygous58224921
3147514748147514749CG1GENIChomozygous58224923
3147514837147514838TG8GENICpossibly homozygous58224924
3147515147147515148TG16GENICpossibly homozygous57727532
3147515592147515593CT16GENIChomozygous58224925
3147517282147517283TG19GENIChomozygous57727542
3147517341147517342AG14GENICheterozygous57727544
3147517344147517345GA13GENIChomozygous57727546
3147517442147517443CT18GENIChomozygous57727550