chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116716401116716405GAGG13GENIChomozygous128635201
8116716619116716620TG19GENIChomozygous116669949
8116717880116717881GT9GENIChomozygous116669951
8116718327116718328AC16GENICpossibly homozygous116669953
8116718387116718388AT15GENIChomozygous116669955
8116718756116718757TC21GENIChomozygous116669957
8116718927116718928AT20GENIChomozygous116669959
8116719284116719285AG13GENIChomozygous116669961
8116721097116721098GA15GENIChomozygous116669969
8116719444116719445GA29GENIChomozygous116669963
8116719639116719640GA15GENIChomozygous116669965
8116719949116719950AG20GENIChomozygous116669967
8116721572116721573AG9GENIChomozygous116669971
8116721971116721972GA20GENIChomozygous116669973
8116722153116722154CT22GENIChomozygous116669975
8116723146116723147GT17GENIChomozygous116669977
8116723187116723188CT12GENIChomozygous116669979
8116724263116724263G35GENIChomozygous128635202
8116724337116724338AG28GENIChomozygous116669983
8116724974116724975TC18GENIChomozygous116669985
8116725236116725237CT20GENIChomozygous116669987
8116725326116725327AG13GENIChomozygous116669989
8116725369116725369G8GENIChomozygous128635203
8116727994116727995TA15GENIChomozygous116669991
8116728564116728565GA22GENIChomozygous116669993
8116729082116729083CT14GENIChomozygous116669995