chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104131597341315974A-29GENIChomozygous754804252
104131597541315976C-29GENIChomozygous754804253
104131597841315979T-28GENIChomozygous754804254
104131623741316238AC46GENIChomozygous646158139
104131638741316388A-47GENICheterozygous754804255
104131639541316396GT47GENICheterozygous646158140
104131643241316433GA32GENIChomozygous646158141
104131644341316444AC30GENIChomozygous646158142
104131645141316452TC33GENIChomozygous646158143
104131648241316483TA23GENIChomozygous646158144
104131649741316498GC22GENIChomozygous646158145
104131662441316625CCAG16GENIChomozygous754804256
104131665241316653AG15GENIChomozygous646158146
104131670941316710A-15GENIChomozygous754804257
104131671341316716GGG---16GENICpossibly homozygous754804258
104131678141316782TG18GENIChomozygous646158147
104131678741316789TC--20GENICpossibly homozygous754804259
104131683141316834GGT---38GENICheterozygous754804260
104131683441316835GGCA37GENICheterozygous754804261
104131693341316934CG16GENICpossibly homozygous646158148
104131702141317022GT46GENICheterozygous646158149
104131709441317095CT24GENIChomozygous646158150
104131709841317099T-26GENICheterozygous754804262
104131710341317104AAC28GENICheterozygous754804263
104131715741317158A-41GENICheterozygous754804264
104131717341317174TTG44GENICheterozygous754804265
104131721441317215CT40GENICheterozygous646158151
104131721541317216CG39GENICheterozygous646158152
104131728241317283AT31GENICheterozygous646158153