chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4105615934105615935TC18GENIChomozygous71094918
4105616015105616016TG20GENIChomozygous71094922
4105616238105616239TG18GENIChomozygous71094926
4105617549105617550TC23GENIChomozygous71094929
4105617964105617965GT17GENIChomozygous71094933
4105618253105618254CT8GENIChomozygous71094937
4105618344105618345AG6GENIChomozygous71094941