chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104131597341315974A-21GENIChomozygous705785728
104131597541315976C-22GENIChomozygous705785729
104131597841315979T-23GENIChomozygous705785730
104131623741316238AC38GENIChomozygous561956662
104131632041316321G-34GENICheterozygous705785731
104131632241316325CTC---35GENICheterozygous705785732
104131638741316388A-50GENICheterozygous705785733
104131639541316396GT44GENICheterozygous561956663
104131643241316433GA34GENIChomozygous560131978
104131644341316444AC28GENIChomozygous560131979
104131645141316452TC26GENIChomozygous561956664
104131648241316483TA22GENIChomozygous561956665
104131649741316498GC23GENIChomozygous561956666
104131662441316625CCAG15GENIChomozygous705785734
104131665241316653AG16GENIChomozygous560131980
104131670941316710A-7GENIChomozygous705785735
104131671341316716GGG---11GENIChomozygous705785736
104131678141316782TG17GENICpossibly homozygous561956667
104131678741316789TC--17GENICpossibly homozygous705785737
104131683141316834GGT---23GENICheterozygous705785738
104131683441316835GGCA23GENICheterozygous705785739
104131702141317022GT50GENICheterozygous560131981
104131709441317095CT36GENIChomozygous560131982
104131709841317099T-38GENICheterozygous705785740
104131710341317104AAC38GENICheterozygous705785741
104131715741317158A-50GENICheterozygous705785742
104131717341317174TTG59GENICheterozygous705785743
104131721441317215CT58GENICheterozygous561956668
104131721541317216CG58GENICheterozygous561956669
104131728241317283AT55GENICpossibly homozygous560131983