chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148427456684274567AG18GENIChomozygous113605550
148427525884275259CA13GENIChomozygous113605551
148427527384275274AG15GENIChomozygous113605552
148427561584275616AG14GENIChomozygous113605553
148427846784278468AG9GENIChomozygous113605554
148427896384278964TC14GENIChomozygous113605555
148428008084280081CT11GENIChomozygous113605556
148428027384280274CT8GENIChomozygous118765986
148428043384280434GA16GENIChomozygous118765987
148428053384280534CT22GENIChomozygous113605557
148428059484280595TG23GENIChomozygous114099312
148428101384281014TA18GENIChomozygous113605558
148428113784281138AG19GENIChomozygous113605559
148428194284281943GA13GENIChomozygous114099313
148428194684281947GA13GENIChomozygous114099314
148428195984281959TG13GENIChomozygous131145519
148428324384283244AC15GENIChomozygous113605560
148428484484284844T14GENIChomozygous131145520
148428484984284849ACCCCCGAGGGCCCCCTTATCTCTG14GENIChomozygous131145521
148428516684285167AG21GENIChomozygous113605561
148428537084285371GA6GENIChomozygous113680097
148428641384286413A18GENIChomozygous131145522
148428670284286703TC19GENIChomozygous113605562
148428671784286718TC22GENIChomozygous113605563
148428945484289455AG19GENIChomozygous113605564
148429000784290008GA16GENIChomozygous113605565
148429019784290198TC14GENIChomozygous113605566