chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144161887144161888CT19GENIChomozygous114036701
5144163041144163042CT19GENIChomozygous114036702
5144163151144163152CA22GENIChomozygous114036703
5144163972144163973CT22GENIChomozygous114036704
5144167565144167566TC16GENIChomozygous114036706
5144169921144169922TC33GENIChomozygous114036707
5144169938144169939AG30GENIChomozygous114036708
5144171171144171172AG28GENIChomozygous114036709
5144171210144171211GC18GENIChomozygous114036710
5144173685144173686CA24GENIChomozygous118846232
5144174710144174711TC12GENIChomozygous114036711
5144175239144175240GT21GENIChomozygous114036712
5144175369144175370GA15GENIChomozygous114036713
5144177340144177341AG11GENIChomozygous114036715
5144177820144177821AG14GENIChomozygous114036716