chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1247522301247522302TC60GENIChomozygous109017665
1247522610247522611AG64GENIChomozygous109017666
1247523046247523047TG64GENIChomozygous109017667
1247523565247523566AT61GENIChomozygous109017668
1247523590247523590A57GENIChomozygous127501468
1247523605247523606TC52GENIChomozygous120515931
1247523625247523625TGTAAGACT44GENIChomozygous131265592
1247524335247524336GT35GENIChomozygous109017669
1247524432247524432AGAAAAGATACTCA40GENICpossibly homozygous131265593
1247524538247524539AC36GENIChomozygous109017670
1247524778247524779AG19GENIChomozygous109017672
1247525392247525392GGGGTGTGTGTGTGTATGAGGGGTGTGTGTGTGTATGAGGGGTGTGTGC15GENIChomozygous127501469
1247525872247525873TC49GENIChomozygous108602911
1247528737247528899ATACACACATACATACACATACATACATACACACATACATACACACATACACACACATACATACATACATATACATACATACATACATACACACATACATACACATACATACATACACACACATACACACACATACACACATACATACATATACATACATAC33GENICheterozygous132541512
1247529063247529077ACATACATACACAT38GENICpossibly homozygous131265594
1247530257247530258AG11GENIChomozygous109017684
1247534313247534314TA53GENIChomozygous108602915
1247537391247537392AG47GENIChomozygous109017703
1247537695247537696CA44GENICpossibly homozygous108602917
1247537884247537885AG34GENIChomozygous108602918
1247538475247538475ATCCATCCATCCATCC33GENIChomozygous131265595
1247539146247539147GA48GENIChomozygous108602919
1247539232247539233CT45GENIChomozygous125470776
1247524207247524208GT48GENIChomozygous120878795
1247524627247524628GA36GENICpossibly homozygous120878796
1247534540247534541TG61GENICpossibly homozygous120878797
1247537129247537130CT44GENIChomozygous120878798
1247528724247528726AT31GENIChomozygous133524960
1247530400247530401GA32GENICheterozygous131284054