chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109577068395770684TG31GENICheterozygous116688144
109577068395770683G31GENICheterozygous130682379
109580307895803078G16GENIChomozygous128848817
109580308295803082G16GENIChomozygous128848818
109580309795803097G13GENICpossibly homozygous128848819
109580310295803102G13GENICpossibly homozygous128848820
109580310795803107G11GENICpossibly homozygous128848821
109580315595803156T13GENIChomozygous128848823
109580315995803159T14GENIChomozygous128848824
109583014295830142A23GENIChomozygous129970562
109583014695830148TG24GENIChomozygous129970563
109583020495830206TG27GENICheterozygous133232975
109585092495850924C41GENIChomozygous128848836
109585094495850944A36GENIChomozygous128848837
109585099195850991T33GENIChomozygous128848838
109585099595850995C32GENIChomozygous128848839
109585107495851075T14GENIChomozygous129970564
109585208295852083T51GENIChomozygous128848841
109586529895865299TC16GENICpossibly homozygous118009693
109589381495893814G53GENIChomozygous128848853
109589829095898290AAATGTGTGCTTAGCAGGAAAGTGTAGGGAGCAAGGAATGACTCCAGCTCTCAGAGCCGGATGCTGCGGGGAGCACATATTTTTGGGAC35GENIChomozygous128848854
109585097695850977CT35GENIChomozygous117328786
109585097895850979TA34GENIChomozygous117328788
109585306295853062A20GENICheterozygous133968640