chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
138397263583972636GC48GENICpossibly homozygous114416684
138397305083973051CT19GENICheterozygous118464464
138397428983974290GA49GENIChomozygous114416686
138397448483974485AG40GENIChomozygous114416688
138397540783975408TG28GENIChomozygous114780022
138397557883975579TC41GENIChomozygous114416690
138397596783975968GA51GENICpossibly homozygous114416692
138397620183976202AG42GENIChomozygous114416694
138397681383976814AC47GENIChomozygous114416696
138397871683978717TC49GENIChomozygous114416698
138397924283979243CA43GENICpossibly homozygous114416700
138397935283979353CT60GENIChomozygous114416702
138398117483981175GA65GENIChomozygous114645694
138398065983980660AG47GENIChomozygous114416704
138398119883981199GT68GENIChomozygous114416706
138398151083981511CT37GENIChomozygous114416708
138398316783983168AG36GENIChomozygous114416710