chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1499648514996486TC12GENIChomozygous108232976
X1499654814996549AT17GENIChomozygous108232978
X1499655914996560AG18GENIChomozygous108232980
X1499685314996854GA7GENIChomozygous108471923
X1499995514999956CT21GENIChomozygous108471925
X1500026915000270CT15GENIChomozygous108232990
X1499756114997562AG10GENIChomozygous108232984
X1499903914999040AC7GENIChomozygous108232986
X1499924514999246AG17GENIChomozygous108232988
X1500136515001366AG5GENIChomozygous108671655
X1500138115001382AT10GENIChomozygous119905693
X1500422415004225AG12GENIChomozygous108232994
X1500425615004257TC16GENIChomozygous108232996
X1500327215003273TC17GENICheterozygous108439104
X1500470615004707GA17GENIChomozygous108471927
X1500529615005297GA15GENIChomozygous108471929
X1500436515004366TC27GENIChomozygous108369806