chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1503602615036027CT16GENIChomozygous108471971
X1503669415036695GC11GENIChomozygous108471973
X1504183115041832CT9GENIChomozygous108233018
X1504231415042315AG13GENIChomozygous108233020
X1504416315044164TG11GENIChomozygous108471976
X1504572915045730GT6GENIChomozygous108471978
X1504575915045760GA7GENIChomozygous108233024
X1504576015045761AG7GENIChomozygous108233026
X1504578415045785GC7GENIChomozygous108233028
X1504578615045787TG7GENIChomozygous108233030
X1504578715045788GC7GENIChomozygous108233032
X1504600315046004TC13GENIChomozygous108471980
X1504663215046633CT5GENIChomozygous108471982
X1504719015047191TG8GENIChomozygous108233034
X1504728215047283CG16GENIChomozygous108233036
X1504729015047291CA15GENIChomozygous108233038
X1504731615047317AG14GENIChomozygous108233040
X1504737415047375GA9GENIChomozygous108233042
X1504738415047385CA10GENIChomozygous108233044
X1504738515047386GA9GENIChomozygous108233046
X1504739215047393CA15GENIChomozygous108233048