Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:45000775-45000961 | Common:1; Rare:78 | ||||
chr10:45374062-45374259 | Common:3; Rare:70 | ||||
chr10:45594867-45594979 | Common:1; Rare:51 | ||||
chr10:45727116-45727307 | Common:3; Rare:73 | ||||
chr10:45972349-45972569 | Common:1; Rare:71 | ||||
chr10:46030530-46030729 | Common:1; Rare:64 | ||||
chr10:46398252-46398424 | Common:3; Rare:69 | ||||
chr10:46911377-46911467 | Rare:7 | ||||
chr10:48306534-48306731 | Common:2; Rare:98 | ||||
chr10:49539023-49539231 | Common:3; Rare:69; Clinvar:2; Clinvar (benign):2 | ||||
chr10:49679549-49679686 | Common:1; Rare:46 | ||||
chr10:49941919-49942115 | Rare:58 | ||||
chr10:50067862-50067990 | Common:2; Rare:59 | ||||
chr10:50623876-50624084 | Common:1; Rare:82 | ||||
chr10:50624875-50624976 | Common:1; Rare:38 |