chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1261504353261504354TC20GENIChomozygous109026094
1261504617261504618TC33GENIChomozygous108629669
1261509298261509299CA13GENIChomozygous109026095
1261509654261509655GA11GENIChomozygous108629680
1261509993261509994CT24GENIChomozygous109026096
1261510247261510248TG17GENIChomozygous109026097
1261510563261510564CT19GENIChomozygous109026098
1261510626261510627CT18GENIChomozygous109026099
1261510712261510713AG14GENIChomozygous109026100
1261512437261512438AG27GENIChomozygous109026103
1261513281261513282CT19GENIChomozygous109026104
1261513422261513423TG20GENIChomozygous109026105
1261514007261514008TC28GENIChomozygous108629686