| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:100903894-100904131 | Common:2; Rare:57 | ||||
| chr14:100907353-100907698 | Common:3; Rare:73 | ||||
| chr14:101562766-101563027 | Common:2; Rare:61 | ||||
| chr14:101948016-101948381 | Common:2; Rare:109 | ||||
| chr14:105481994-105482205 | Common:1; Rare:55 | ||||
| chr15:22887540-22887825 | Common:1; Rare:55 | ||||
| chr15:25785275-25785580 | Common:4; Rare:84 | ||||
| chr15:25850574-25850682 | Common:5; Rare:35 | ||||
| chr15:32701380-32701634 | Common:6; Rare:53 | ||||
| chr15:34795432-34795594 | Common:2; Rare:45; Clinvar:4; Clinvar (benign):4 | ||||
| chr15:34813033-34813245 | Rare:50 | ||||
| chr15:35061563-35061793 | Rare:43 | ||||
| chr15:39584045-39584422 | Common:1; Rare:103 | ||||
| chr15:39918794-39918966 | Common:1; Rare:25 | ||||
| chr15:41283816-41284021 | Common:1; Rare:54 |