chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X7683126076831261GA4GENIChomozygous129818949
X7694274776942748TC9GENIChomozygous108818180
X7694274876942749GA9GENIChomozygous108818181
X7685262876852629AC8GENIChomozygous108275008
X7685262976852630AT8GENIChomozygous108275010
X7685265476852655GA5GENIChomozygous108275012
X7685907776859077C8GENIChomozygous129757045
X7693763476937635T11GENIChomozygous129757046
X7693765576937656C11GENIChomozygous129757047
X7694272676942727TC9GENIChomozygous119928826
X7696830876968322ACATGTGGAAAGGA1GENIChomozygous129757050
X7697480976974809C3GENIChomozygous129757053
X7697482376974823CC3GENIChomozygous129757054
X7697484376974844T2GENIChomozygous129757055
X7697484876974848C2GENIChomozygous129757056
X7697847476978474CCCC4GENIChomozygous129757057
X7697847676978476CC4GENIChomozygous129757058
X7697848076978480C4GENIChomozygous129757059
X7697849076978491TC3GENIChomozygous120003568
X7697849676978496CC3GENIChomozygous129757060
X7697850476978504C3GENIChomozygous129757061
X7697851576978515G2GENIChomozygous129757062
X7697852076978520C2GENIChomozygous129757063
X7697851176978512CA2GENIChomozygous108766791
X7696825676968257CT2GENIChomozygous108608645