chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
87380998873809989TTA2GENICheterozygous52998236
87381010373810105TG--9GENIChomozygous53301750
87381350473813505CT21GENIChomozygous53213951
87381415373814154AG21GENIChomozygous53125113
87381467173814672TC9GENICpossibly homozygous53301752
87381536673815367TC2GENIChomozygous53301753
87381612773816128AG21GENICpossibly homozygous53301755
87381707773817078TG2GENIChomozygous53301756
87382042373820424CT3GENIChomozygous53301757
87382287773822878TG11GENIChomozygous53301758
87382883773828838CT10GENIChomozygous53301759
87383165673831657TA7GENIChomozygous53301760
87383249473832495CA1GENIChomozygous53301761
87383411173834112TG17GENIChomozygous53301762
87383667073836671CT8GENICpossibly homozygous53301764
87383674873836749CT22GENIChomozygous53301765
87384081473840815TC16GENIChomozygous53301766
87384233373842334GA17GENICpossibly homozygous53301767
87384385973843861AG--2GENICheterozygous53395979
87385090073850901TC14GENIChomozygous53301768
87385473573854736T-2GENIChomozygous53301769
87385869473858695TC20GENICpossibly homozygous53301770
87385927473859275A-3GENIChomozygous53395980
87392775173927752AT1GENIChomozygous52676636
87392781373927814AG1GENIChomozygous53301772
87383940473839405A-3GENICheterozygous53537333