chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2066334856633486A14GENIChomozygous140483920
2066336586633659CA17GENIChomozygous130037575
2066337286633729CT31GENIChomozygous140512719
2066337846633785GA30GENIChomozygous140512720
2066338556633856CG27GENIChomozygous130037576
2066348326634832T18GENIChomozygous140483921
2066356776635678AG16GENIChomozygous130037579
2066358266635827TC15GENIChomozygous130037580
2066370456637046AT15GENIChomozygous130037581
2066341446634148GGGT16GENIChomozygous129980651
2066366386636638GACAT10GENIChomozygous129980653
2066379196637920TC17GENIChomozygous130037582
2066379826637983TC16GENIChomozygous130037583
2066383196638320AG15GENIChomozygous130037585
2066385106638511GC3GENIChomozygous140512721
2066390936639093A14GENIChomozygous140483922
2066391096639114AAAAG14GENIChomozygous140483923
2066392586639259CG13GENIChomozygous130037588
2066410356641035TCC7GENIChomozygous140483925
2066411466641147AG12GENIChomozygous130037592
2066417246641725AC16GENIChomozygous130037594
2066418756641876TC27GENIChomozygous130037595