| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41367181-41367483 | Rare:86 | ||||
| chr22:41446790-41446958 | Rare:67 | ||||
| chr22:41468620-41468800 | Common:2; Rare:46 | ||||
| chr22:41468972-41469175 | Rare:70 | ||||
| chr22:41560903-41561127 | Common:9; Rare:65 | ||||
| chr22:41620988-41621380 | Common:7; Rare:140 | ||||
| chr22:41800506-41800702 | Common:1; Rare:61 | ||||
| chr22:41832909-41833355 | Common:3; Rare:149 | ||||
| chr22:41947093-41947225 | Rare:50 | ||||
| chr22:42070770-42070977 | Common:3; Rare:44 | ||||
| chr22:42079491-42079778 | Common:2; Rare:77 | ||||
| chr22:42090607-42091020 | Common:2; Rare:173; Clinvar (pathogenic):1 | ||||
| chr22:42130863-42131026 | Common:1; Rare:45 | ||||
| chr22:42614829-42615246 | Common:3; Rare:179 | ||||
| chr22:42649303-42649482 | Common:1; Rare:68 |