chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X7120057071200571C5GENICheterozygous130719987
X7121812871218131GAG2GENIChomozygous129753930
X7121810771218108GC2GENIChomozygous129817469
X7121809271218093T1GENIChomozygous129753925
X7121809771218098G1GENIChomozygous129753926
X7121811071218111G2GENIChomozygous129753927
X7121811771218118C2GENIChomozygous129753928
X7121812371218124C2GENIChomozygous129753929
X7121813371218134G2GENIChomozygous129753931
X7121814271218142C2GENIChomozygous129753932
X7121814471218145G2GENIChomozygous129753933
X7121814671218148AG2GENIChomozygous129753934
X7121815971218161TG3GENIChomozygous129753935
X7121816671218167G3GENIChomozygous129753936
X7121816871218169G3GENIChomozygous129753937
X7121817571218175C3GENIChomozygous129753938
X7121823471218238GCCG6GENIChomozygous129753939
X7121825771218257T7GENIChomozygous129753940
X7121831471218315C11GENIChomozygous129753941
X7121832371218324G13GENIChomozygous129753942
X7121835071218351C13GENIChomozygous129753943
X7122255971222560T9GENICheterozygous131969836
X7122261571222616T7GENICheterozygous131969837
X7122712371227124T8GENICheterozygous131969838
X7121813571218136CT2GENIChomozygous108677230
X7121822571218226CG6GENIChomozygous108391239
X7121822671218227GC6GENIChomozygous108391241
X7121823871218239CT6GENIChomozygous108391243