chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123205396332053964AG16GENIChomozygous139130574
123205416532054166AG27GENIChomozygous139130575
123205444732054448GA12GENIChomozygous139130576
123205478132054782CT18GENIChomozygous139130577
123205516032055163CCC14GENIChomozygous139052327
123205537832055379AC15GENICheterozygous403644918
123205516032055161CT14GENICheterozygous154746123
123205516032055161C14GENIChomozygous403324842
123205537732055378A15GENIChomozygous403644915
123205537732055378AC15GENICheterozygous403644916
123205537832055379A15GENIChomozygous403644917
123205538732055388AC15GENIChomozygous139130578
123205546532055466AT15GENIChomozygous139130579
123205547632055476T15GENIChomozygous139052328
123205580232055802ACTG12GENIChomozygous139052329
123205587832055879TC13GENIChomozygous139130580
123205588132055882CG12GENIChomozygous139130581
123205656732056568CT14GENICpossibly homozygous139130582
123205658232056583GC13GENIChomozygous139130583
123205674332056744AG27GENIChomozygous139130584
123205702732057028TC16GENIChomozygous139130585
123205725732057257T19GENIChomozygous139052330
123205737432057375TC24GENIChomozygous139130586
123205737532057376GA24GENIChomozygous139130587
123205763732057638CT23GENIChomozygous139130588
123205768632057687TG20GENIChomozygous139130589
123205804132058042GA12GENIChomozygous139130590
123205806332058064AG14GENIChomozygous139130591
123205817532058176AG22GENIChomozygous139130592
123205849132058491A20GENIChomozygous139052331
123205860732058608AG11GENIChomozygous139130593
123205871432058717TTC15GENIChomozygous139052332
123205893432058935CA23GENIChomozygous139130594
123205934132059342GC16GENIChomozygous139130595
123205939732059398CG25GENIChomozygous139130596
123205971132059712CG17GENIChomozygous139130597
123205990532059905C25GENIChomozygous139052333
123205992532059926AG26GENIChomozygous139130598
123206115532061156GT14GENIChomozygous139130599
123205538632055387AC15GENICheterozygous404402298
123205538632055387A15GENIChomozygous404402297