| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24212984-24213198 | Rare:36 | ||||
| chr14:24232314-24232995 | Common:9; Rare:161 | ||||
| chr14:24233382-24233597 | Common:1; Rare:75 | ||||
| chr14:24241794-24241909 | Rare:34 | ||||
| chr14:24242222-24242422 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24242559-24242751 | Common:1; Rare:43; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24271366-24271831 | Common:3; Rare:123 | ||||
| chr14:24299125-24299332 | Common:1; Rare:45 | ||||
| chr14:24299633-24300199 | Common:7; Rare:197 | ||||
| chr14:24314483-24314951 | Rare:83 | ||||
| chr14:24429861-24430340 | Common:4; Rare:114 | ||||
| chr14:24430358-24430655 | Rare:48 | ||||
| chr14:24442650-24443056 | Common:5; Rare:125 | ||||
| chr14:30622036-30622395 | Common:1; Rare:123 | ||||
| chr14:30734634-30734856 | Common:1; Rare:42 |