chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120718603120718604TC13GENIChomozygous116081947
7120718728120718729GA6GENIChomozygous116081948
7120720857120720858GA12GENIChomozygous116081950
7120725260120725261TC8GENIChomozygous116081951
7120725358120725359AT7GENIChomozygous118259119
7120725618120725619CG5GENIChomozygous116081952
7120725758120725759CT11GENIChomozygous116081953
7120726101120726102CT15GENIChomozygous115856964
7120726485120726486TC11GENIChomozygous115856966
7120732091120732092TA15GENIChomozygous115856970
7120732334120732335TG7GENIChomozygous115856972
7120733282120733283TC12GENIChomozygous115856974
7120739059120739060CG4GENIChomozygous115856976
7120739176120739177AC7GENIChomozygous115856978
7120739713120739714AC9GENIChomozygous115856980
7120741078120741079GA5GENIChomozygous115856982
7120741738120741739CT4GENIChomozygous115856984
7120741757120741758GA4GENIChomozygous115856986