chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1515595215155953TA19GENIChomozygous108542382
X1515637515156376TC27GENIChomozygous108233148
X1515715715157158TC19GENIChomozygous108542384
X1515764215157643TG21GENICpossibly homozygous108542386
X1515828415158285TC27GENIChomozygous108233152
X1515850515158506GA15GENIChomozygous108542388
X1515856315158564AT9GENIChomozygous108542390
X1515935915159360GA15GENIChomozygous108233154
X1515994115159942C20GENIChomozygous129722488
X1515995115159952G20GENIChomozygous129722489
X1516085015160851AT21GENIChomozygous108542392
X1516090915160910CT19GENIChomozygous108542394
X1516218815162189CT23GENIChomozygous108233156
X1515953015159530A9GENIChomozygous134976694
X1516209215162095AAC17GENICheterozygous134976695
X1516200915162010CT18GENIChomozygous120536307
X1515954015159541TA8GENIChomozygous134977948
X1515955115159552AG6GENIChomozygous120023030
X1516203515162036AG19GENIChomozygous120023031
X1515996315159964CG18GENIChomozygous108562904
X1516000215160003GT12GENIChomozygous108562906
X1516002815160029TG14GENIChomozygous108562908
X1516014615160147TC17GENIChomozygous108562910
X1516003815160039TC13GENIChomozygous108653870
X1516008815160089TC13GENIChomozygous108439110
X1516204815162049GC21GENIChomozygous133358822