chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5152064783152064784CT21GENIChomozygous55926578
5152065667152065668GA9GENIChomozygous56291637
5152065689152065693TCTC----8GENIChomozygous56461042
5152065718152065742GTGTGTGTGTGTGTGTGAGAGAGA------------------------7GENIChomozygous56461043
5152065764152065765GGT10GENIChomozygous55798230
5152065962152065963TTG1GENIChomozygous55798238
5152066033152066034GGTGTGTGTT18GENICheterozygous56461044
5152066195152066196TC3GENICheterozygous55798245
5152066206152066222TGTGTGTGTGTGTGTG----------------3GENICheterozygous56494992
5152066223152066224GC3GENICheterozygous56494993
5152066263152066264AG5GENIChomozygous55798247
5152066449152066450CCTG24GENIChomozygous55798249
5152067046152067047GA31GENIChomozygous55926588
5152067174152067175CT17GENIChomozygous55926590
5152067773152067774AG17GENIChomozygous55798254
5152067920152067921GA12GENIChomozygous55926592
5152068196152068197TC23GENIChomozygous55798259
5152068198152068199AC23GENIChomozygous55798260
5152068925152068935ACACACACAC----------6GENICheterozygous56494994
5152068927152068935ACACACAC--------6GENICheterozygous56461046
5152069458152069459GGAAA13GENIChomozygous55926594
5152069514152069515A-7GENICheterozygous55798262
5152071291152071292AG21GENIChomozygous55798265
5152071396152071397CCTG10GENICpossibly homozygous56461047
5152071539152071540AC10GENIChomozygous55798267
5152071892152071893CT21GENIChomozygous55926598
5152072371152072379GGAAGGAA--------9GENICheterozygous56554516
5152072375152072379GGAA----9GENICpossibly homozygous56461048
5152073001152073002AG14GENIChomozygous55926602
5152073077152073078AG12GENIChomozygous55798268
5152073116152073117TC12GENIChomozygous55798269
5152073567152073568TC11GENIChomozygous55798271