| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:54396691-54397132 | Common:2; Rare:116 | ||||
| chr14:54440951-54441128 | Common:1; Rare:63 | ||||
| chr14:54441228-54441488 | Rare:97 | ||||
| chr14:54488758-54489241 | Common:4; Rare:122 | ||||
| chr14:54509593-54509968 | Common:6; Rare:134 | ||||
| chr14:54566935-54567260 | Rare:84 | ||||
| chr14:54567494-54567819 | Common:2; Rare:62 | ||||
| chr14:54567956-54568211 | Common:1; Rare:62 | ||||
| chr14:54776376-54776519 | Common:3; Rare:45 | ||||
| chr14:54901895-54902351 | Common:4; Rare:131; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr14:54902679-54902988 | Common:3; Rare:95; Clinvar:3; Clinvar (benign):4 | ||||
| chr14:55026927-55027516 | Common:4; Rare:135 | ||||
| chr14:55027687-55027897 | Common:1; Rare:45 | ||||
| chr14:55051392-55051811 | Common:2; Rare:172 | ||||
| chr14:55051923-55052199 | Common:1; Rare:85 |