chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X104765127104765128TC14GENIChomozygous45325970
X104768838104768839TTC11INTERGENIChomozygous45189995
X104769651104769652GA7INTERGENIChomozygous45325971
X104771293104771294AG12INTERGENIChomozygous45325972
X104771461104771462GA6INTERGENIChomozygous45325973
X104771592104771593GC9INTERGENIChomozygous45325974
X104771594104771595CA9INTERGENIChomozygous45325975
X104771924104771925TC6INTERGENIChomozygous45325976
X104772650104772651TG4INTERGENIChomozygous45325977
X104776488104776489TG3INTERGENIChomozygous45325978
X104778965104778966TG4INTERGENIChomozygous45325979
X104780465104780466GA11INTERGENIChomozygous45325980
X104780637104780638GGCA2INTERGENICheterozygous45668962
X104798175104798176CT5INTERGENIChomozygous45325982
X104799165104799166CT12INTERGENIChomozygous45325983
X104799483104799484GA7INTERGENIChomozygous45325984
X104801979104801980CT7INTERGENIChomozygous45325985
X104802743104802744CCAAA13GENIChomozygous45189996
X104802746104802747CCA14GENIChomozygous45189997
X104804525104804526GA8GENIChomozygous45325986
X104805188104805189CT17GENIChomozygous45325987
X104807232104807233A-6GENIChomozygous45668963
X104807381104807382TTTGTG5GENICheterozygous45668964
X104807382104807384TG--5GENICheterozygous45519601
X104808541104808542CCA13GENIChomozygous45325990
X104808847104808848GGT12GENICheterozygous45550177
X104809416104809442TCTCTCTCTCTCTCTCTCTCTCTCTC--------------------------5GENIChomozygous45668965
X104809816104809817AG8GENIChomozygous45325991
X104809981104809982AC9GENIChomozygous45325992
X104810098104810099GGTGTA5GENIChomozygous45325993
X104811553104811557TCTC----1GENIChomozygous45668966
X104811915104811916GA7GENIChomozygous45325994
X104812151104812152CT11GENIChomozygous45325995
X104778527104778528AC2INTERGENIChomozygous45614206