chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6111177069111177070GA23GENIChomozygous115225590
6111177117111177118GT28GENIChomozygous115225591
6111177378111177379CT8GENIChomozygous115225592
6111177785111177785AATA16GENIChomozygous131413506
6111177814111177815GA16GENIChomozygous115225593
6111179928111179931CGG10GENIChomozygous134556458
6111181528111181529CT29GENIChomozygous114940445
6111177683111177684AG20GENIChomozygous115276967
6111181494111181495AC31GENIChomozygous115276969
6111180834111180835CT22GENIChomozygous114940443
6111181076111181077A22GENIChomozygous128381709
6111182682111182683GA18GENIChomozygous115276971
6111183431111183431AGTGACTCAGTAGACCAGCATAGTGTAAACAGAACTCTTCATAACACCGAGAAACAAAGTCTATGTAAATTGCTTTATTCCCAAACCTGCTATTTTCTCTAGTCTGGACTTAACCCCCTATCTCCACAGCATACCAATACTAGGATTCTTGAGAAGTTTGTGTTTTGTTTTTAA20GENICpossibly homozygous128381710
6111183594111183595AG25GENIChomozygous114940447
6111184233111184234GA22GENIChomozygous115276973
6111185033111185034GA27GENIChomozygous114940451
6111185055111185056TC24GENIChomozygous114940452
6111185091111185092GT27GENIChomozygous114940453
6111185766111185769GGT35GENIChomozygous128381711
6111186273111186274AG18GENIChomozygous114940454
6111186512111186513AG19GENIChomozygous114940455
6111187161111187162TC10GENIChomozygous114940456