chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117937084117937085GC18GENICpossibly homozygous563888005
8117937113117937114GA16GENICpossibly homozygous563888006
8117937599117937600TC16GENIChomozygous563888007
8117938840117938841CA3GENICheterozygous565288079
8117938845117938846G-2GENIChomozygous708469393
8117938987117938989TC--18GENICpossibly homozygous708469394
8117948034117948035TC14GENIChomozygous563888008
8117948142117948143TC28GENICpossibly homozygous563888009
8117948689117948690A-1GENIChomozygous708469395
8117952317117952318G-3GENICheterozygous708469396
8117952318117952319GT3GENICheterozygous563888010
8117952320117952321TC3GENICheterozygous565288080
8117954073117954074CT17GENIChomozygous563888011
8117956795117956796CG2GENIChomozygous565288081
8117960587117960588GA16GENIChomozygous563888012
8117960691117960694GGG---8GENIChomozygous708469398
8117962115117962116AG30GENICpossibly homozygous563888013
8117963462117963463T-7GENICheterozygous708469399
8117963771117963772AG22GENICpossibly homozygous563888014
8117968702117968703TG4GENIChomozygous563888015
8117969150117969151TC12GENIChomozygous563888016
8117969446117969447AG10GENICpossibly homozygous563888017
8117969914117969915TTG16GENICpossibly homozygous708469400
8117972274117972275T-3GENIChomozygous708469401