chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
159737032097370321CT33GENIChomozygous112605535
159737100697371007AG23GENIChomozygous112756699
159737491697374917CA14GENIChomozygous112605537
159737530397375304TG14GENIChomozygous112756701
159737532397375324AC14GENIChomozygous112756703
159737566097375661AT24GENIChomozygous112605543
159737574297375743AG12GENIChomozygous112605545
159737575297375753TC14GENIChomozygous112756705
159737575397375754CA14GENIChomozygous112756707
159737592297375923CT17GENIChomozygous112756709
159737616497376165GA19GENIChomozygous112756711
159737631697376317TA10GENIChomozygous112756713
159737631797376318GA10GENIChomozygous112756715
159737723297377233CT25GENIChomozygous112605557
159737733697377337TA22GENIChomozygous112756723