| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41468945-41469175 | Rare:77 | ||||
| chr22:41544575-41544875 | Common:4; Rare:69 | ||||
| chr22:41560889-41561132 | Common:9; Rare:68 | ||||
| chr22:41621009-41621370 | Common:7; Rare:133 | ||||
| chr22:41832909-41833295 | Common:3; Rare:138 | ||||
| chr22:41947026-41947255 | Common:1; Rare:78 | ||||
| chr22:42070775-42071006 | Common:3; Rare:50 | ||||
| chr22:42079632-42079783 | Common:1; Rare:46 | ||||
| chr22:42090723-42090993 | Common:1; Rare:106; Clinvar (pathogenic):1 | ||||
| chr22:42614846-42615244 | Common:3; Rare:163 | ||||
| chr22:42857215-42857430 | Common:2; Rare:89 | ||||
| chr22:43089327-43089507 | Common:3; Rare:57 | ||||
| chr22:43143318-43143477 | Common:2; Rare:57 | ||||
| chr22:43955253-43955587 | Common:4; Rare:97 | ||||
| chr22:44024178-44024345 | Common:1; Rare:58 |