| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41367239-41367498 | Rare:77 | ||||
| chr22:41446778-41446980 | Rare:85 | ||||
| chr22:41468606-41468792 | Common:2; Rare:48 | ||||
| chr22:41468939-41469149 | Rare:60 | ||||
| chr22:41621018-41621396 | Common:7; Rare:139 | ||||
| chr22:41800475-41800720 | Common:1; Rare:79 | ||||
| chr22:41832849-41833355 | Common:3; Rare:168 | ||||
| chr22:42070775-42070977 | Common:3; Rare:42 | ||||
| chr22:42079634-42079827 | Common:1; Rare:65 | ||||
| chr22:42090607-42091110 | Common:2; Rare:192; Clinvar (pathogenic):1 | ||||
| chr22:42519753-42519962 | Common:1; Rare:84 | ||||
| chr22:42553628-42553978 | Common:3; Rare:102 | ||||
| chr22:42614820-42615244 | Common:3; Rare:181 | ||||
| chr22:42649297-42649482 | Common:1; Rare:69 | ||||
| chr22:42876395-42876439 | Rare:13 |