chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X128156736128156737TC9GENIChomozygous125119904
X128156884128156885GA10GENIChomozygous125119905
X128159507128159508TC16GENIChomozygous125119906
X128164782128164783CT10GENIChomozygous125119907
X128165023128165024GA8GENIChomozygous125119908
X128168294128168295TC12GENIChomozygous125119909
X128176872128176873GC7GENIChomozygous125119911
X128186731128186732GT7GENIChomozygous125136931
X128189718128189719TC8GENIChomozygous125119912
X128193167128193168CT10GENIChomozygous125119913
X128207951128207952TA15GENIChomozygous125119915
X128211289128211290CG8GENIChomozygous125136932
X128211332128211333GT10GENIChomozygous125119916
X128214822128214823TC7GENIChomozygous125119917
X128237010128237011TG9GENIChomozygous125119918
X128241196128241197CT15GENIChomozygous125119919
X128241449128241450TC4GENIChomozygous125119920
X128243333128243334CT11GENIChomozygous125136933
X128243498128243499AG6GENIChomozygous125119921
X128251089128251090AG10GENIChomozygous125119922
X128252864128252865TC11GENIChomozygous125119923
X128253216128253217TC12GENIChomozygous125119924
X128254202128254203GA15GENIChomozygous125119925
X128256812128256813AC3GENICheterozygous125119927
X128258244128258245AG11GENIChomozygous125119928
X128258580128258581AG14GENIChomozygous125119929
X128259499128259500AG10GENIChomozygous125119930
X128260789128260790CG14GENIChomozygous125136934
X128262469128262470TA8GENIChomozygous125136935
X128264556128264557CA9GENIChomozygous125119931
X128266330128266331TG3GENICheterozygous125136936