chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X104764149104764150GA10GENICheterozygous45311008
X104765127104765128TC15GENIChomozygous45325970
X104769651104769652GA7INTERGENIChomozygous45325971
X104771293104771294AG12INTERGENIChomozygous45325972
X104771461104771462GA6INTERGENIChomozygous45325973
X104771592104771593GC9INTERGENIChomozygous45325974
X104771594104771595CA9INTERGENIChomozygous45325975
X104771924104771925TC6INTERGENIChomozygous45325976
X104772650104772651TG4INTERGENIChomozygous45325977
X104776488104776489TG4INTERGENIChomozygous45325978
X104778965104778966TG4INTERGENIChomozygous45325979
X104780465104780466GA11INTERGENIChomozygous45325980
X104782706104782707TA2INTERGENIChomozygous45325981
X104798175104798176CT5INTERGENIChomozygous45325982
X104799165104799166CT11INTERGENIChomozygous45325983
X104799483104799484GA7INTERGENIChomozygous45325984
X104801979104801980CT12INTERGENIChomozygous45325985
X104804525104804526GA9GENIChomozygous45325986
X104805188104805189CT18GENIChomozygous45325987
X104807089104807090CT13GENICheterozygous45325988
X104807092104807093CA12GENICheterozygous45325989
X104768496104768497AG4INTERGENICheterozygous45264098
X104768512104768513GA4INTERGENICheterozygous45264099
X104768838104768839TTC12INTERGENIChomozygous45189995
X104802743104802744CCAAA9GENIChomozygous45189996
X104802746104802747CCA7GENIChomozygous45189997
X104808541104808542CCA15GENIChomozygous45325990
X104809816104809817AG8GENIChomozygous45325991
X104809981104809982AC9GENIChomozygous45325992
X104810098104810099GGTGTA8GENIChomozygous45325993
X104811915104811916GA7GENIChomozygous45325994
X104812151104812152CT11GENIChomozygous45325995