chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4175294878175294879TC65GENIChomozygous145529876
4175296003175296004CT44GENIChomozygous145529877
4175297149175297150GA47GENIChomozygous145529878
4175297229175297230GA52GENIChomozygous145529879
4175298135175298136GT46GENIChomozygous145529880
4175300818175300819CT39GENIChomozygous145529881
4175300985175300986GA31GENICpossibly homozygous145529882
4175301410175301411TC39GENIChomozygous145529883
4175305597175305598GC46GENIChomozygous137271689
4175306653175306654TC43GENIChomozygous145529884
4175306713175306714AG47GENIChomozygous145529885
4175307094175307098CCCA19GENIChomozygous145452791
4175299534175299534G14GENIChomozygous145452788
4175301544175301544G44GENIChomozygous145452789
4175305061175305063AG34GENIChomozygous145452790
4175307118175307120CT21GENIChomozygous145452792
4175309506175309507AG61GENIChomozygous137271691
4175309563175309564TG59GENICpossibly homozygous137271692
4175310027175310028TG61GENIChomozygous145529886
4175311020175311022TG50GENIChomozygous145452793
4175307097175307098A21GENIChomozygous403992898
4175307097175307098AC21GENICheterozygous403992899