chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
159737032097370321CT12GENIChomozygous112605535
159737100697371007AG22GENIChomozygous112756699
159737491697374917CA10GENIChomozygous112605537
159737530397375304TG19GENIChomozygous112756701
159737532397375324AC14GENIChomozygous112756703
159737566097375661AT16GENIChomozygous112605543
159737574297375743AG8GENIChomozygous112605545
159737575297375753TC7GENIChomozygous112756705
159737575397375754CA9GENIChomozygous112756707
159737592297375923CT22GENIChomozygous112756709
159737616497376165GA14GENIChomozygous112756711
159737723297377233CT9GENIChomozygous112605557
159737733697377337TA25GENIChomozygous112756723
159737489197374892GA3GENICheterozygous125858049