chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7121216039121216040TC25GENIChomozygous116225113
7121216540121216541T26GENICpossibly homozygous131433743
7121219627121219628TG24GENIChomozygous116225115
7121220402121220404AG16GENIChomozygous131433744
7121221512121221513AG22GENIChomozygous116225116
7121221952121221953AG27GENIChomozygous116225117
7121224631121224632GA25GENIChomozygous118321938
7121216978121216979GA27GENIChomozygous118418033
7121217552121217553AG23GENIChomozygous118418034
7121218065121218066AG19GENIChomozygous118418035
7121218535121218536AG26GENIChomozygous115858106
7121223317121223318CT17GENIChomozygous115858110
7121221329121221329AC17GENIChomozygous128512707
7121228566121228566ACAGAC12GENIChomozygous128512708
7121228748121228752GCCT26GENIChomozygous131433745
7121229898121229898C11GENIChomozygous131433746
7121231601121231602AG21GENIChomozygous115858130
7121226093121226094AG21GENIChomozygous115858112
7121227221121227222AG24GENIChomozygous115858114
7121227630121227631AC15GENIChomozygous115858116
7121229029121229030AT21GENIChomozygous115858124