chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108934125489341255CT47GENICheterozygous781536999
108934191189341912AG61GENIChomozygous781537000
108934338689343387AG51GENIChomozygous781537001
108934367489343675CT66GENICpossibly homozygous781537002
108934414389344144AG35GENIChomozygous781537003
108934466889344669GA74GENIChomozygous781537004
108934523189345232GA55GENICpossibly homozygous781537005
108934561589345616GC76GENIChomozygous781537006
108934608789346088AT24GENIChomozygous781537007
108934612189346122TC22GENIChomozygous781537008
108934668089346681CT57GENICpossibly homozygous781537009
108934699089346991TC67GENICpossibly homozygous781537010
108934822789348228AG72GENIChomozygous781537011
108934825989348260CT63GENIChomozygous781537012
108934854189348542GA72GENIChomozygous781537013
108934863289348633GA62GENIChomozygous781537014
108934864889348649CT56GENIChomozygous781537015
108934868889348689TC51GENICpossibly homozygous781537016
108934897189348972AC64GENIChomozygous781537017
108934901089349011GA64GENIChomozygous781537018
108934917489349175TC72GENIChomozygous781537019
108934918689349187CG70GENICpossibly homozygous781537020