| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40951618-40951716 | Common:1; Rare:25 | ||||
| chr22:41091418-41091758 | Common:5; Rare:119 | ||||
| chr22:41286122-41286424 | Common:2; Rare:98 | ||||
| chr22:41468657-41468773 | Common:2; Rare:32 | ||||
| chr22:41468939-41469175 | Rare:78 | ||||
| chr22:41621012-41621370 | Common:7; Rare:133 | ||||
| chr22:41800378-41800708 | Common:3; Rare:91 | ||||
| chr22:41832838-41833209 | Common:3; Rare:121 | ||||
| chr22:41947114-41947196 | Rare:25 | ||||
| chr22:42070782-42071026 | Common:3; Rare:53 | ||||
| chr22:42079630-42079763 | Common:1; Rare:40 | ||||
| chr22:42090710-42090955 | Common:2; Rare:100; Clinvar (pathogenic):1 | ||||
| chr22:42614844-42615246 | Common:3; Rare:168 | ||||
| chr22:42649322-42649479 | Common:1; Rare:62 | ||||
| chr22:42857129-42857471 | Common:3; Rare:135 |