| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23953661-23953813 | Common:6; Rare:53 | ||||
| chr14:23988775-23988943 | Common:8; Rare:70 | ||||
| chr14:24093976-24094356 | Common:4; Rare:97 | ||||
| chr14:24114998-24115280 | Common:2; Rare:78 | ||||
| chr14:24141529-24141862 | Common:1; Rare:79 | ||||
| chr14:24146553-24146887 | Common:1; Rare:106 | ||||
| chr14:24195309-24195359 | Rare:16 | ||||
| chr14:24195400-24195729 | Common:2; Rare:73 | ||||
| chr14:24213062-24213198 | Rare:27 | ||||
| chr14:24213417-24213621 | Common:1; Rare:68 | ||||
| chr14:24232289-24232714 | Common:8; Rare:107 | ||||
| chr14:24232816-24232954 | Common:1; Rare:29 | ||||
| chr14:24242258-24242401 | Rare:51; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:24242580-24242774 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24271457-24271611 | Common:1; Rare:46 |