chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1515544515155446TC20GENIChomozygous108233146
X1515637515156376TC25GENIChomozygous108233148
X1515752315157525AC29GENIChomozygous129722486
X1515771815157719GT30GENIChomozygous108233150
X1515828415158285TC28GENIChomozygous108233152
X1515856215158562TAAAAAGTAGATGGGGGCTGGAGAGATGGCTCAGCCGTTAAAGGCTAGGCTCACAACCAAAAATA16GENIChomozygous129722487
X1515935915159360GA13GENIChomozygous108233154
X1515994115159942C21GENIChomozygous129722488
X1515995115159952G22GENIChomozygous129722489
X1515996315159964CG22GENIChomozygous108562904
X1516000215160003GT18GENIChomozygous108562906
X1516002815160029TG16GENIChomozygous108562908
X1516014615160147TC26GENIChomozygous108562910
X1516003815160039TC16GENIChomozygous108653870
X1516008815160089TC19GENIChomozygous108439110
X1516162315161624TA9GENICheterozygous132254076
X1516164115161642GC10GENICheterozygous108630777
X1516202915162030TC16GENIChomozygous119905735
X1516203915162040GA16GENIChomozygous119905736
X1516218815162189CT23GENIChomozygous108233156
X1516252215162523G22GENIChomozygous129722490
X1516375815163759CT35GENIChomozygous108233158