chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1503669415036695GC4GENIChomozygous108471973
X1504183115041832CT20GENIChomozygous108233018
X1504231415042315AG12GENIChomozygous108233020
X1504600315046004TC10GENIChomozygous108471980
X1504663215046633CT9GENIChomozygous108471982
X1504719015047191TG10GENIChomozygous108233034
X1504728215047283CG8GENIChomozygous108233036
X1504729015047291CA6GENIChomozygous108233038
X1504731615047317AG8GENIChomozygous108233040
X1504737415047375GA6GENIChomozygous108233042
X1504738415047385CA5GENIChomozygous108233044
X1504738515047386GA5GENIChomozygous108233046
X1504739215047393CA5GENIChomozygous108233048
X1504621815046219TA14GENIChomozygous108595057