chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106204491162044912TC14GENIChomozygous116613299
106204589662045897GA18GENIChomozygous117295804
106205292462052925GA12GENIChomozygous117295808
106205425262054253CT10GENIChomozygous117295810
106206208462062085TA22GENIChomozygous117295812
106206455862064559CT8GENIChomozygous117295814
106207241962072420GA18GENIChomozygous116939567
106207364062073641CT14GENIChomozygous116613309
106207814362078144GA11GENIChomozygous116939571
106208162062081621GA26GENIChomozygous116939573
106208248462082485CT17GENIChomozygous116939575
106208249562082496CT18GENIChomozygous116939577
106208318162083182AG14GENIChomozygous117295816
106208549462085495TG29GENIChomozygous116613326
106208632762086328GA19GENIChomozygous117295818
106208767562087676CA14GENIChomozygous116613330
106208884262088843GA21GENIChomozygous117295820
106208916962089170TC16GENIChomozygous116613334
106209184862091849CT15GENIChomozygous117295822
106209244962092450GA10GENIChomozygous117295824
106209313362093134AG16GENIChomozygous116613338
106210247262102473GA13GENIChomozygous116613342
106210345062103451CG8GENIChomozygous116613344
106210394662103947CT21GENIChomozygous116613346
106210421162104212TC22GENIChomozygous117295826
106210522962105230GA14GENIChomozygous117295828
106210592762105928TC13GENIChomozygous117295830
106210597762105978TG9GENIChomozygous116613348
106210874362108744GC13GENIChomozygous116613350