| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41446785-41446945 | Rare:63 | ||||
| chr22:41468611-41468813 | Common:2; Rare:53 | ||||
| chr22:41468965-41469175 | Rare:72 | ||||
| chr22:41620751-41620766 | Rare:5 | ||||
| chr22:41621005-41621401 | Common:7; Rare:147 | ||||
| chr22:41800528-41800688 | Common:1; Rare:50 | ||||
| chr22:41832909-41833319 | Common:3; Rare:143 | ||||
| chr22:42070775-42070963 | Common:2; Rare:39 | ||||
| chr22:42079497-42079771 | Common:2; Rare:74 | ||||
| chr22:42090607-42090956 | Common:2; Rare:148; Clinvar (pathogenic):1 | ||||
| chr22:42130863-42130930 | Rare:22 | ||||
| chr22:42614838-42615256 | Common:3; Rare:183 | ||||
| chr22:42649297-42649482 | Common:1; Rare:69 | ||||
| chr22:42959799-42959987 | Common:1; Rare:34 | ||||
| chr22:43812279-43812437 | Common:2; Rare:53 |