chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71108679211086793TC8GENIChomozygous68595900
71109039911090400AC16GENIChomozygous68595902
71109044111090442CT12GENIChomozygous68595904
71109480411094805CA24GENIChomozygous68595907
71109490311094904GA14GENIChomozygous68595909
71109509211095093GA17GENIChomozygous68595912
71109558811095589GA24GENIChomozygous68595914
71109828711098288AG25GENIChomozygous68595925
71109856311098564AG25GENICpossibly homozygous68595928
71110022611100227CG4GENIChomozygous68595929
71110028611100287GA8GENIChomozygous68595932
71110067411100675CT8GENIChomozygous68595935
71110115311101154CT11GENIChomozygous68595937
71110116611101167GC10GENIChomozygous68595940
71110126311101264CG22GENIChomozygous68595943
71110182611101827CA5GENIChomozygous68595965
71110183411101835GA7GENIChomozygous68595968
71110281911102820GA4GENIChomozygous69839428
71110170811101708G9GENIChomozygous70327482