chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174481580444815805TC37GENICheterozygous119289886
174481587944815880GA77GENICheterozygous119289887
174481588444815885GA80GENICheterozygous119289888
174481590344815904GA78GENICheterozygous119341939
174481593044815931GA80GENICheterozygous119289889
174481598144815982GA70GENICheterozygous119289890
174481599044815991AC73GENICheterozygous119289891
174481814144818142CT50GENIChomozygous111054246
174481943644819437GA56GENIChomozygous111054248
174482017744820178TC49GENIChomozygous111054250
174482151944821520GA16GENICheterozygous111402481
174482168844821689GA29GENICheterozygous119289893
174482169444821695GA26GENICheterozygous119289894
174482381044823811TC34GENIChomozygous111672133
174482453744824538GA34GENIChomozygous111244836
174482653144826532TC46GENICheterozygous119389811
174482659144826592GA30GENIChomozygous111054252
174482690444826905AC43GENIChomozygous111054254
174482851144828512CT44GENICpossibly homozygous111054256
174482873544828736AG48GENIChomozygous111054258
174482924444829245AG70GENICheterozygous119289895
174482924944829250TG73GENICheterozygous119289896
174482925544829256CA77GENICheterozygous119289897
174482925744829258CT78GENICheterozygous119289898
174482927244829273GA97GENICheterozygous119289899
174482929444829295AG111GENICheterozygous119289900
174482932544829326GC101GENICheterozygous119289901
174482934144829342GA98GENICheterozygous119289902
174482935244829353TG98GENICheterozygous111054260
174482935944829360AT90GENICheterozygous111054262
174482937044829371AT77GENICheterozygous119389813
174482937644829377GA63GENICheterozygous119389815
174483132944831330TC41GENIChomozygous111054264
174483140244831403GA42GENIChomozygous111054266
174483329144833292TC42GENIChomozygous111054268
174483566844835669AG104GENICheterozygous119289903
174483579944835800GA34GENIChomozygous119289904
174483784444837845AG61GENIChomozygous111054270
174483923744839238CG48GENICpossibly homozygous111054272
174483980244839803CT40GENIChomozygous119289906