chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1499648514996486TC9GENIChomozygous108232976
X1499654814996549AT8GENIChomozygous108232978
X1499655914996560AG8GENIChomozygous108232980
X1499685314996854GA10GENIChomozygous108471923
X1499756114997562AG13GENIChomozygous108232984
X1499903914999040AC8GENIChomozygous108232986
X1499924514999246AG16GENIChomozygous108232988
X1499995514999956CT17GENIChomozygous108471925
X1500026915000270CT9GENIChomozygous108232990
X1500422415004225AG11GENIChomozygous108232994
X1500425615004257TC12GENIChomozygous108232996
X1500436515004366TC7GENIChomozygous108369806
X1500470615004707GA14GENIChomozygous108471927
X1500529615005297GA12GENIChomozygous108471929
X1500327215003273TC7GENIChomozygous108439104
X1500136515001366AG9GENICheterozygous108671655
X1500138115001382AT9GENICheterozygous119905693