| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24114916-24115330 | Common:2; Rare:117 | ||||
| chr14:24141486-24141819 | Common:2; Rare:80 | ||||
| chr14:24146587-24146683 | Rare:39 | ||||
| chr14:24171846-24172093 | Common:3; Rare:55 | ||||
| chr14:24195400-24195744 | Common:2; Rare:76 | ||||
| chr14:24213072-24213198 | Rare:24 | ||||
| chr14:24232289-24232680 | Common:8; Rare:102 | ||||
| chr14:24232734-24232942 | Common:1; Rare:45 | ||||
| chr14:24242262-24242421 | Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:24242524-24242680 | Common:1; Rare:36; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:24299701-24299854 | Common:4; Rare:44 | ||||
| chr14:24429861-24429980 | Rare:28 | ||||
| chr14:24442659-24442877 | Common:2; Rare:87 | ||||
| chr14:24442890-24443013 | Common:3; Rare:25 | ||||
| chr14:25049901-25050281 | Common:3; Rare:128 |