chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
138397263583972636GC48GENIChomozygous114416684
138397275983972759GCTTGCTAGGCAAGCGCTCTACCACTGAGCTAAATCCC17GENIChomozygous130419114
138397428983974290GA56GENIChomozygous114416686
138397448483974485AG53GENIChomozygous114416688
138397540783975408TG19GENIChomozygous114780022
138397557883975579TC26GENIChomozygous114416690
138397596783975968GA24GENIChomozygous114416692
138397620183976202AG34GENIChomozygous114416694
138397681383976814AC61GENICpossibly homozygous114416696
138397871683978717TC55GENIChomozygous114416698
138397924283979243CA32GENIChomozygous114416700
138397935283979353CT35GENIChomozygous114416702
138397310183973102CT11GENICheterozygous129113276
138397328283973283T46GENIChomozygous129080840
138398065983980660AG59GENIChomozygous114416704
138398119883981199GT49GENIChomozygous114416706
138398151083981511CT55GENIChomozygous114416708
138398254283982542TACCTGAACCCT59GENIChomozygous129080841
138398266383982665CC23GENIChomozygous129080842
138398316783983168AG50GENIChomozygous114416710
138398117483981175GA52GENIChomozygous114645694
138398274683982758AGAGAGAGAGAA13GENICheterozygous132172997