chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X104765127104765128TC10GENICheterozygous45325970
X104769651104769652GA12INTERGENICheterozygous45325971
X104771293104771294AG10INTERGENICheterozygous45325972
X104771592104771593GC12INTERGENICheterozygous45325974
X104771594104771595CA12INTERGENICheterozygous45325975
X104771924104771925TC12INTERGENICheterozygous45325976
X104778965104778966TG9INTERGENICheterozygous45325979
X104782706104782707TA10INTERGENICheterozygous45325981
X104798175104798176CT14INTERGENICheterozygous45325982
X104799165104799166CT8INTERGENICheterozygous45325983
X104799483104799484GA8INTERGENICheterozygous45325984
X104804525104804526GA9GENICheterozygous45325986
X104809816104809817AG9GENICheterozygous45325991
X104812151104812152CT9GENICheterozygous45325995