| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:36320550-36320785 | Common:4; Rare:83 | ||||
| chr14:37172561-37172646 | Common:1; Rare:37 | ||||
| chr14:37197834-37198082 | Common:3; Rare:83 | ||||
| chr14:38207959-38208225 | Rare:60 | ||||
| chr14:38256077-38256313 | Common:1; Rare:57 | ||||
| chr14:39175035-39175303 | Common:4; Rare:97 | ||||
| chr14:39266475-39266699 | Common:2; Rare:70 | ||||
| chr14:39432456-39432624 | Common:6; Rare:56 | ||||
| chr14:44961845-44962255 | Common:3; Rare:125 | ||||
| chr14:45253161-45253279 | Rare:29 | ||||
| chr14:49586347-49586776 | Common:1; Rare:230 | ||||
| chr14:49598711-49598996 | Common:1; Rare:106 | ||||
| chr14:49599162-49599183 | Rare:9 | ||||
| chr14:49620564-49620933 | Common:3; Rare:136; Clinvar:6; Clinvar (benign):1 | ||||
| chr14:49635127-49635153 | Rare:10; Clinvar (benign):1 |