chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116730584116730585TC23GENIChomozygous116669997
8116732257116732258AG31GENIChomozygous116669999
8116732398116732399CT29GENICheterozygous116988154
8116732410116732411CT31GENICheterozygous116988155
8116734175116734176TC20GENIChomozygous116670001
8116734212116734213AG22GENIChomozygous116670003
8116735667116735668AT5GENIChomozygous116670005
8116735729116735730AG10GENIChomozygous116670007
8116735864116735865AG10GENIChomozygous116670011
8116736861116736862AG17GENIChomozygous116670013
8116737034116737035GA31GENIChomozygous116670015
8116737506116737507TC20GENICpossibly homozygous116670017
8116737616116737617TG17GENIChomozygous116670019
8116737900116737901CT30GENIChomozygous116670021
8116738694116738695GA19GENIChomozygous116670023
8116740312116740313AG21GENIChomozygous116670025
8116740733116740734CT19GENIChomozygous116670027
8116741370116741371GA20GENIChomozygous116670029
8116742066116742067TC28GENIChomozygous116670031
8116742439116742440TC28GENIChomozygous116670033
8116742572116742573GA24GENIChomozygous116670035
8116742642116742643TC24GENIChomozygous116670037
8116742821116742822CT24GENIChomozygous116670039
8116743569116743570CT19GENIChomozygous116670041
8116743664116743665GA29GENIChomozygous116670043
8116743882116743883TC13GENIChomozygous116670045
8116744846116744847CT23GENIChomozygous116670047
8116744965116744966AT22GENIChomozygous116670049
8116745460116745461AG25GENIChomozygous116670051
8116745509116745510GA23GENIChomozygous116670053
8116746034116746035CT17GENIChomozygous116670055
8116746461116746462GA12GENIChomozygous116670057
8116746767116746768CT18GENIChomozygous116670059
8116746965116746966GA11GENIChomozygous116670061
8116749652116749653CT24GENIChomozygous116670069
8116747885116747886GA15GENIChomozygous116670063
8116748297116748298GA25GENIChomozygous116670065
8116748523116748524GA27GENIChomozygous116670067
8116749994116749995AG23GENIChomozygous116670071
8116750338116750339AT23GENIChomozygous116670073