chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109577068395770684TG14GENICpossibly homozygous116688144
109579967895799678T14GENICheterozygous128848813
109580307895803078G4GENIChomozygous128848817
109580308295803082G4GENIChomozygous128848818
109580315995803159T6GENIChomozygous128848824
109580309795803097G4GENIChomozygous128848819
109580310295803102G4GENIChomozygous128848820
109580310795803107G4GENIChomozygous128848821
109580315595803156T6GENIChomozygous128848823
109583014295830142A9GENIChomozygous129970562
109583014695830148TG9GENIChomozygous129970563
109584675695846758GT6GENICheterozygous128848835
109585092495850924C19GENIChomozygous128848836
109585094495850944A16GENIChomozygous128848837
109585099195850991T10GENIChomozygous128848838
109585099595850995C10GENIChomozygous128848839
109585107495851075T5GENIChomozygous129970564
109585208295852083T15GENIChomozygous128848841
109586529895865299TC7GENICheterozygous118009693
109589381495893814G16GENIChomozygous128848853
109589829095898290AAATGTGTGCTTAGCAGGAAAGTGTAGGGAGCAAGGAATGACTCCAGCTCTCAGAGCCGGATGCTGCGGGGAGCACATATTTTTGGGAC18GENIChomozygous128848854
109584939395849437GTGTAATGTGGTATGGTATTTGTTGTTATGATGTATGTATTGTA4GENICheterozygous130394479
109585097695850977CT10GENIChomozygous117328786
109585097895850979TA10GENIChomozygous117328788