chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104131597341315974A-31GENIChomozygous715057748
104131597541315976C-31GENIChomozygous715057749
104131597841315979T-32GENIChomozygous715057750
104131598541315986T-37GENICheterozygous715057751
104131623741316238AC31GENIChomozygous603978105
104131632041316321G-28GENICheterozygous715057752
104131632241316325CTC---30GENICheterozygous715057753
104131638741316388A-40GENICheterozygous715057754
104131639541316396GT42GENICheterozygous603978106
104131643241316433GA40GENIChomozygous576626329
104131644341316444AC42GENIChomozygous576626330
104131645141316452TC40GENIChomozygous603978107
104131648241316483TA31GENIChomozygous603978108
104131649741316498GC30GENIChomozygous603978109
104131662441316625CCAG14GENIChomozygous715057755
104131665241316653AG13GENIChomozygous576626331
104131670941316710A-9GENIChomozygous715057756
104131671341316716GGG---10GENIChomozygous715057757
104131678141316782TG20GENICpossibly homozygous603978110
104131678741316789TC--22GENICpossibly homozygous715057758
104131683141316834GGT---37GENICheterozygous715057759
104131683441316835GGCA38GENICheterozygous715057760
104131702141317022GT34GENICheterozygous576626332
104131709441317095CT27GENIChomozygous576626333
104131709841317099T-27GENICheterozygous715057761
104131710341317104AAC27GENICheterozygous715057762
104131715741317158A-34GENICheterozygous715057763
104131717341317174TTG38GENICheterozygous715057764
104131721441317215CT31GENICheterozygous603978111
104131721541317216CG32GENICheterozygous603978112
104131728241317283AT36GENIChomozygous576626334