| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40856479-40856717 | Rare:110 | ||||
| chr22:40856755-40857159 | Common:2; Rare:151; Clinvar:3 | ||||
| chr22:41286158-41286557 | Common:2; Rare:125 | ||||
| chr22:41301425-41301640 | Rare:64 | ||||
| chr22:41446791-41446980 | Rare:80 | ||||
| chr22:41468984-41469159 | Rare:58 | ||||
| chr22:41621006-41621385 | Common:7; Rare:137 | ||||
| chr22:41621705-41622086 | Common:1; Rare:99 | ||||
| chr22:41800506-41800724 | Common:1; Rare:68 | ||||
| chr22:41832909-41833223 | Common:3; Rare:105 | ||||
| chr22:41946713-41946949 | Common:3; Rare:59 | ||||
| chr22:41947093-41947194 | Rare:37 | ||||
| chr22:42070770-42070945 | Common:1; Rare:37 | ||||
| chr22:42090658-42090945 | Common:2; Rare:129; Clinvar (pathogenic):1 | ||||
| chr22:42614811-42615246 | Common:4; Rare:190 |