| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:95024793-95025109 | Common:2; Rare:114; Clinvar:1; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr8:95268718-95268837 | Common:7; Rare:29 | ||||
| chr8:95269198-95269329 | Common:6; Rare:52; Clinvar:1 | ||||
| chr8:96235510-96235727 | Common:1; Rare:108; Clinvar (benign):2 | ||||
| chr8:96261566-96261998 | Common:6; Rare:142 | ||||
| chr8:97644715-97644881 | Common:1; Rare:54 | ||||
| chr8:97868911-97869224 | Common:3; Rare:63 | ||||
| chr8:98021054-98021306 | Common:2; Rare:48 | ||||
| chr8:98045345-98045666 | Common:3; Rare:97 | ||||
| chr8:98117144-98117333 | Common:4; Rare:61 | ||||
| chr8:98942556-98942687 | Rare:30 | ||||
| chr8:98948642-98948831 | Common:2; Rare:47 | ||||
| chr8:99012679-99012891 | Rare:37 | ||||
| chr8:99013007-99013368 | Rare:76; Clinvar:1 | ||||
| chr8:100150565-100150699 | Rare:42 |