chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123205292632052928AG19GENIChomozygous143522939
123205362332053624GA20GENIChomozygous143542620
123205396332053964AG19GENIChomozygous139130574
123205416532054166AG22GENIChomozygous139130575
123205444732054448GA18GENIChomozygous139130576
123205478132054782CT30GENIChomozygous139130577
123205537632055376C5GENIChomozygous143522940
123205546532055466AT20GENIChomozygous139130579
123205580232055802ACTG12GENIChomozygous139052329
123205516032055163CCC26GENIChomozygous139052327
123205547632055476T21GENIChomozygous139052328
123205587832055879TC15GENIChomozygous139130580
123205588132055882CG15GENIChomozygous139130581
123205656732056568CT21GENIChomozygous139130582
123205658232056583GC20GENIChomozygous139130583
123205674332056744AG12GENIChomozygous139130584
123205702732057028TC11GENIChomozygous139130585
123205725732057257T18GENIChomozygous139052330
123205737432057375TC13GENIChomozygous139130586
123205763732057638CT19GENIChomozygous139130588
123205768632057687TG19GENIChomozygous139130589
123205804132058042GA16GENIChomozygous139130590
123205806332058064AG18GENIChomozygous139130591
123205817532058176AG18GENIChomozygous139130592
123205860732058608AG10GENIChomozygous139130593
123205893432058935CA16GENIChomozygous139130594
123205934132059342GC19GENIChomozygous139130595
123205938832059389GA19GENIChomozygous143542621
123205939732059398CG19GENIChomozygous139130596
123205971132059712CG24GENIChomozygous139130597
123205982732059828AG18GENIChomozygous143542622
123205990532059905C29GENIChomozygous139052333
123205992532059926AG29GENIChomozygous139130598
123206122332061224GT15GENIChomozygous143542623
123205516032055161C26GENIChomozygous403324842
123205516032055161CT26GENICheterozygous154746123