| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41367186-41367483 | Rare:86 | ||||
| chr22:41446440-41446542 | Rare:18 | ||||
| chr22:41446778-41446980 | Rare:85 | ||||
| chr22:41468939-41469159 | Rare:67 | ||||
| chr22:41560908-41561139 | Common:9; Rare:67 | ||||
| chr22:41621006-41621370 | Common:7; Rare:134 | ||||
| chr22:41800506-41800697 | Common:1; Rare:60 | ||||
| chr22:41832909-41833145 | Common:3; Rare:77 | ||||
| chr22:42070768-42071035 | Common:3; Rare:61 | ||||
| chr22:42079604-42079763 | Common:1; Rare:50 | ||||
| chr22:42090607-42091049 | Common:2; Rare:177; Clinvar (pathogenic):1 | ||||
| chr22:42519782-42519962 | Common:1; Rare:67 | ||||
| chr22:42614849-42615251 | Common:3; Rare:169 | ||||
| chr22:42649308-42649482 | Common:1; Rare:68 | ||||
| chr22:42856731-42857034 | Common:2; Rare:86 |