| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41468480-41469170 | Common:2; Rare:191 | ||||
| chr22:41544561-41544876 | Common:4; Rare:76 | ||||
| chr22:41589865-41590223 | Common:6; Rare:114 | ||||
| chr22:41620998-41621388 | Common:7; Rare:141 | ||||
| chr22:41832876-41833355 | Common:3; Rare:159 | ||||
| chr22:41946420-41946626 | Common:1; Rare:89 | ||||
| chr22:41946702-41946949 | Common:3; Rare:62 | ||||
| chr22:41947015-41947231 | Common:1; Rare:79 | ||||
| chr22:42079632-42079823 | Common:1; Rare:64 | ||||
| chr22:42090730-42091031 | Common:1; Rare:109; Clinvar (pathogenic):1 | ||||
| chr22:42614801-42615244 | Common:5; Rare:188 | ||||
| chr22:42649314-42649484 | Common:1; Rare:67 | ||||
| chr22:43089332-43089646 | Common:3; Rare:89 | ||||
| chr22:44024115-44024366 | Common:2; Rare:78 | ||||
| chr22:44676664-44676867 | Common:1; Rare:38 |