chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97960234879602349CT36GENIChomozygous117578568
97960474179604742T7GENIChomozygous128726873
97960473579604736G8GENIChomozygous128726872
97960381879603818TG15GENIChomozygous128726870
97960382279603822TATTTGTTTTGGTGTTGTTGGGTTTTTTGGGGGGTGTGGGG15GENIChomozygous128726871
97960475179604752G7GENIChomozygous128726874
97960475379604754G7GENIChomozygous128726875
97960475679604757C6GENIChomozygous128726876
97960476479604765G6GENIChomozygous128726877
97960477679604777G4GENIChomozygous128726878
97960563479605635GT22GENIChomozygous117578580
97960476779604768AG5GENIChomozygous117380740
97960686579606866AG14GENICheterozygous134342275
97961090479610905AG25GENIChomozygous117729478
97961260179612601TG18GENIChomozygous131071448
97961432179614321G14GENIChomozygous131071449
97961815479618155GA16GENICpossibly homozygous117748487
97961832679618327GT21GENIChomozygous117729480
97961835779618358GC17GENIChomozygous117578608
97961880979618809A11GENIChomozygous131071451
97961897579618975G25GENIChomozygous131071452
97961963879619639AG13GENIChomozygous117729482
97961979979619800TG22GENIChomozygous117729484
97962053979620540AG19GENIChomozygous117729486
97962065279620653AG20GENIChomozygous117729488
97962110179621102AG22GENIChomozygous117578612
97962130679621307TA29GENIChomozygous117380743
97962130779621308TG29GENIChomozygous117380744
97962240179622402CT14GENIChomozygous117729492
97962091479620915CT16GENIChomozygous117729490
97962243579622436GA15GENIChomozygous117729494
97962255979622560TC9GENIChomozygous117578616
97962283679622837GA19GENIChomozygous117729496
97962340679623407A19GENIChomozygous130677192
97962486179624862CA10GENIChomozygous117748498
97962487979624880AG10GENIChomozygous117748499
97962552379625524TC25GENIChomozygous117729498
97962606679626067CT22GENIChomozygous117729500
97962637379626374TG15GENIChomozygous117578626
97962642679626427GA13GENIChomozygous117578630
97962644779626448TC14GENICpossibly homozygous117578632
97962645579626455CATA17GENICpossibly homozygous131071453
97962675879626759CA14GENICpossibly homozygous117578634
97962729079627293TTC10GENIChomozygous131071454
97962731079627311CG14GENIChomozygous117578636
97962734179627342GT12GENIChomozygous117578638
97962766679627667CG16GENIChomozygous117578642
97962796679627966AAC13GENIChomozygous131071455
97962805179628052AT12GENIChomozygous117578644
97962850479628505TC10GENIChomozygous117578646
97962856579628566AC8GENIChomozygous117578648
97962877579628776CA21GENIChomozygous117578650
97962883279628833CT20GENIChomozygous117578652
97962909079629091CT26GENIChomozygous117578654
97962926279629263CT22GENIChomozygous117578656
97962944379629444GA18GENIChomozygous117578658
97962952979629530A22GENIChomozygous131071457
97962961979629620C21GENICpossibly homozygous131071458
97962968079629681AT12GENIChomozygous117578660
97962595079625951TC25GENIChomozygous117794123
97962969279629693CT13GENIChomozygous117578662