chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124190810441908105TC16GENIChomozygous139145586
124190864341908644GA18GENIChomozygous139145587
124190876441908765TC23GENICpossibly homozygous139145588
124190902741909028GA17GENIChomozygous139145589
124190935241909353TC18GENIChomozygous139145590
124190956841909569CT13GENIChomozygous139145591
124190979041909791GA15GENIChomozygous139145592
124191053941910540CT13GENIChomozygous139145593
124191064941910650CT11GENIChomozygous139145594
124191088241910882CTG17GENIChomozygous139056991
124191119041911191CT17GENIChomozygous139145595
124191148441911485CT13GENIChomozygous139145596
124191165641911657CT15GENIChomozygous139145597
124191273541912736TC15GENIChomozygous139145598
124191275341912754GA17GENIChomozygous139145599
124191276441912765TC21GENIChomozygous139145600
124191288741912887C15GENIChomozygous139056992
124191374841913749GA12GENIChomozygous139145601
124191533741915338TC12GENIChomozygous139145602
124191562941915630AC13GENIChomozygous139145603
124191595541915956AG10GENIChomozygous139145604
124191636241916363TG14GENIChomozygous139145605
124191811241918113AC19GENIChomozygous139145606
124191925741919258GT17GENIChomozygous139145607
124192006941920070CT10GENIChomozygous139145608
124192204341922047ACTT22GENIChomozygous139056993
124192217741922178GA22GENIChomozygous139145609
124192286141922862CT23GENIChomozygous139145610
124192293941922939TCTCTCTCTCTCTCTCTCTC3GENIChomozygous147462061
124192320641923207GA18GENICpossibly homozygous139145611
124192361041923611GA24GENIChomozygous139145612
124192363941923640TC28GENIChomozygous139145613
124192443441924435TA16GENIChomozygous139145614