chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
826819802681981TG11GENICpossibly homozygous547399669
826839712683972TC2GENIChomozygous547399670
826840892684090TG3GENIChomozygous547399671
826849112684912GA1GENIChomozygous548624307
826850182685019CT10GENIChomozygous547399672
826869182686919TC15GENICpossibly homozygous548624308
826888562688857GA6GENIChomozygous548624309
826893082689309TC14GENIChomozygous547399673
826902662690267CT10GENIChomozygous547399674
826922312692232T-5GENICheterozygous699087890
826944932694494CT12GENICpossibly homozygous548624310
826946482694649AAT2GENIChomozygous699087891
826979702697971TA5GENIChomozygous547399675
826996302699631CT15GENIChomozygous548624311
827018162701817CT12GENIChomozygous548624312
827047862704787GA28GENIChomozygous548624313
827069732706974AG16GENICpossibly homozygous548624314
827079192707920T-1GENIChomozygous699087892
827080432708044CT4GENIChomozygous548624315
827081802708181TC18GENIChomozygous548624316
827101582710159TG5GENIChomozygous548624317