chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1503669415036695GC7GENIChomozygous108471973
X1504077115040772G6GENIChomozygous129722346
X1504183115041832CT5GENIChomozygous108233018
X1504231415042315AG11GENIChomozygous108233020
X1504534515045345GA12GENIChomozygous129722347
X1504535315045354C12GENIChomozygous129722348
X1504537115045371T12GENIChomozygous129722349
X1504542615045427A11GENIChomozygous129722350
X1504543615045436A9GENIChomozygous129722351
X1504544915045450AT5GENIChomozygous108766286
X1504545315045454T6GENIChomozygous129722352
X1504545515045456CG6GENIChomozygous120536135
X1504549315045493G5GENIChomozygous129722353
X1504558515045585C11GENIChomozygous129722354
X1504560415045605C8GENIChomozygous129722355
X1504562015045621T8GENIChomozygous129722356
X1504566215045663A7GENIChomozygous129722357
X1504567115045672T9GENIChomozygous129722358
X1504569115045692A8GENIChomozygous129722359
X1504570615045707C9GENIChomozygous129722360
X1504571715045718C9GENIChomozygous129722361
X1504572915045730GT8GENIChomozygous108471978
X1504575915045760GA8GENIChomozygous108233024
X1504576015045761AG8GENIChomozygous108233026
X1504576415045765G8GENIChomozygous129722362
X1504578415045785GC8GENIChomozygous108233028
X1504578615045787TG8GENIChomozygous108233030
X1504578715045788GC8GENIChomozygous108233032
X1504719015047191TG7GENIChomozygous108233034
X1504724815047249C13GENIChomozygous129722364
X1504728215047283CG13GENIChomozygous108233036
X1504729015047291CA12GENIChomozygous108233038
X1504731615047317AG11GENIChomozygous108233040
X1504737415047375GA10GENIChomozygous108233042
X1504738415047385CA8GENIChomozygous108233044
X1504738515047386GA8GENIChomozygous108233046
X1504739215047393CA10GENIChomozygous108233048
X1504535615045357GA13GENIChomozygous131770802
X1504539815045399GA11GENIChomozygous119905696
X1504551615045517TG4GENIChomozygous119905697
X1504564015045641GT8GENIChomozygous108618320
X1504584815045849AT5GENIChomozygous108562890