chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71108679211086793TC30GENIChomozygous68595900
71109558811095589GA25GENIChomozygous68595914
71109801611098017GA12GENIChomozygous68595920
71109856311098564AG24GENIChomozygous68595928
71110022611100227CG17GENIChomozygous68595929
71110067411100675CT25GENIChomozygous68595935
71110110611101107AG26GENIChomozygous70505063
71109493711094938TC29GENIChomozygous70505038
71109507811095079AG30GENIChomozygous70505042
71109599911096000GA27GENIChomozygous70505046
71109604211096043AG25GENIChomozygous70505051
71109730911097310TC26GENIChomozygous70505055
71110153811101539CT6GENIChomozygous68595955
71110156711101568AG6GENIChomozygous68595960
71110157811101579CT5GENIChomozygous68595963
71110214311102144AC20GENIChomozygous68595970
71110217711102178CT24GENIChomozygous68595973
71110337411103375TC4GENIChomozygous68595976
71110149311101494AG4GENIChomozygous82006924
71110170711101708CG13GENIChomozygous69957184