chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X139085858139085859GA10GENIChomozygous45235721
X139088639139088640AG12GENIChomozygous45235724
X139090273139090274TC10GENIChomozygous45235727
X139091916139091917GA18GENIChomozygous45235728
X139092457139092458GA9GENIChomozygous45235729
X139095480139095481AG7GENIChomozygous45235730
X139095535139095536GC7GENIChomozygous45235731
X139097280139097281CA8GENIChomozygous45235736
X139097473139097474GGT7GENIChomozygous45235737
X139101247139101248TTA14GENIChomozygous45235740
X139104798139104799AC14GENIChomozygous45235742
X139105036139105037TC11GENIChomozygous45235743
X139105074139105075CT12GENIChomozygous45235744
X139106407139106408AG8GENIChomozygous45235750
X139107658139107659AT7GENIChomozygous45235752
X139109235139109236AG10GENIChomozygous45235754
X139111138139111139TTC8GENIChomozygous45235758
X139111288139111289A-8GENIChomozygous45235759
X139111919139111920TC7GENIChomozygous45235761
X139112219139112220AG8GENIChomozygous45235763
X139112518139112519CT11GENIChomozygous45235764
X139112873139112874TA13GENIChomozygous45235765
X139113334139113340ATACAT------8GENIChomozygous45235767
X139114637139114638GT8GENIChomozygous45235769
X139115265139115266TC15GENIChomozygous45235770
X139117335139117336CCA8GENIChomozygous45235772
X139117383139117384CT8GENIChomozygous45235773
X139117829139117830GGAAT9GENIChomozygous45235774
X139118357139118358AT8GENIChomozygous45235775
X139120240139120241AG10GENIChomozygous45235777
X139123268139123269TA9GENIChomozygous45235782
X139128929139128930G-7GENIChomozygous45235787
X139128951139128952TA10GENIChomozygous45235788