chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X21031402103141AG26GENIChomozygous45076445
X21038142103815CT19GENIChomozygous45076446
X21039292103935GCCGCC------2GENIChomozygous45250204
X21041062104107AG10GENIChomozygous45076447
X21045362104537GA17GENICpossibly homozygous45076448
X21062282106229GA31GENIChomozygous45076449
X21078262107827AG29GENIChomozygous45076450
X21083232108324GA16GENIChomozygous45076451
X21084032108407ACAC----6GENICheterozygous45542278
X21084052108407AC--6GENICheterozygous45496752
X21096972109704AGACTCT-------21GENIChomozygous45076452
X21104862110489AAA---6GENICheterozygous45496755
X21104872110489AA--6GENICheterozygous45496757
X21108092110810GGGATA5GENIChomozygous45710287
X21117802111781TTAAAA5GENIChomozygous45076455
X21128722112873G-12GENICpossibly homozygous45076456
X21136162113617AG25GENIChomozygous45076457
X21142372114238A-14GENIChomozygous45076458
X21159852115986AG29GENIChomozygous45076459
X21194172119418GA18GENIChomozygous45076460
X21195272119528TTC19GENIChomozygous45076461