| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38952611-38952743 | Rare:21 | ||||
| chr22:39319596-39319750 | Common:3; Rare:75 | ||||
| chr22:39349810-39350017 | Common:1; Rare:65 | ||||
| chr22:39399638-39399805 | Common:3; Rare:66 | ||||
| chr22:39502131-39502412 | Rare:84 | ||||
| chr22:40346441-40346580 | Rare:62; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:40636656-40637014 | Common:2; Rare:98 | ||||
| chr22:40679232-40679494 | Rare:59 | ||||
| chr22:40819288-40819499 | Common:11; Rare:106 | ||||
| chr22:40856721-40857179 | Common:3; Rare:170; Clinvar:4 | ||||
| chr22:40951600-40951716 | Common:1; Rare:34 | ||||
| chr22:41286158-41286424 | Common:2; Rare:82 | ||||
| chr22:41301216-41301627 | Common:1; Rare:110 | ||||
| chr22:41381944-41382014 | Rare:39 | ||||
| chr22:41468638-41468810 | Common:2; Rare:48 |