chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
159737032097370321CT11GENIChomozygous112605535
159737100697371007AG11GENIChomozygous112756699
159737491697374917CA10GENIChomozygous112605537
159737530397375304TG12GENIChomozygous112756701
159737532397375324AC9GENIChomozygous112756703
159737566097375661AT20GENIChomozygous112605543
159737574297375743AG9GENIChomozygous112605545
159737592297375923CT8GENIChomozygous112756709
159737616497376165GA5GENIChomozygous112756711
159737631697376317TA5GENIChomozygous112756713
159737631797376318GA5GENIChomozygous112756715
159737723297377233CT15GENIChomozygous112605557
159737733697377337TA9GENIChomozygous112756723
159737168297371683AC7GENICheterozygous118931821