| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40636631-40636996 | Common:2; Rare:108 | ||||
| chr22:40856839-40857150 | Common:2; Rare:119; Clinvar:3 | ||||
| chr22:40951146-40951401 | Common:2; Rare:83 | ||||
| chr22:41091413-41091841 | Common:6; Rare:158 | ||||
| chr22:41446760-41446935 | Rare:68 | ||||
| chr22:41468620-41468792 | Common:2; Rare:45 | ||||
| chr22:41469045-41469148 | Rare:40 | ||||
| chr22:41560932-41561137 | Common:9; Rare:63 | ||||
| chr22:41621015-41621385 | Common:7; Rare:135 | ||||
| chr22:41800545-41800631 | Rare:22 | ||||
| chr22:41832909-41833292 | Common:3; Rare:137 | ||||
| chr22:42070770-42071087 | Common:3; Rare:70 | ||||
| chr22:42079604-42079738 | Common:1; Rare:40 | ||||
| chr22:42090607-42090956 | Common:2; Rare:148; Clinvar (pathogenic):1 | ||||
| chr22:42614844-42615251 | Common:3; Rare:172 |