| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41446795-41446940 | Rare:55 | ||||
| chr22:41468973-41469144 | Rare:49 | ||||
| chr22:41621012-41621368 | Common:7; Rare:133 | ||||
| chr22:41621710-41622011 | Common:1; Rare:82 | ||||
| chr22:41800486-41800702 | Common:1; Rare:71 | ||||
| chr22:41832662-41832739 | Rare:15 | ||||
| chr22:41832909-41833267 | Common:3; Rare:129 | ||||
| chr22:41946731-41946905 | Common:3; Rare:36 | ||||
| chr22:41947093-41947225 | Rare:50 | ||||
| chr22:42070782-42070991 | Common:3; Rare:43 | ||||
| chr22:42079485-42079763 | Common:2; Rare:72 | ||||
| chr22:42090658-42091060 | Common:2; Rare:164; Clinvar (pathogenic):1 | ||||
| chr22:42519779-42519928 | Common:1; Rare:54 | ||||
| chr22:42614858-42615251 | Common:3; Rare:165 | ||||
| chr22:42649329-42649482 | Common:1; Rare:60 |