| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40951031-40951413 | Common:2; Rare:133 | ||||
| chr22:41286175-41286423 | Common:2; Rare:74 | ||||
| chr22:41446784-41446980 | Rare:84 | ||||
| chr22:41468986-41469159 | Rare:58 | ||||
| chr22:41544593-41544871 | Common:4; Rare:65 | ||||
| chr22:41560927-41561102 | Common:9; Rare:55 | ||||
| chr22:41621006-41621370 | Common:7; Rare:134 | ||||
| chr22:41800517-41800685 | Common:1; Rare:54 | ||||
| chr22:41832849-41833146 | Common:3; Rare:97 | ||||
| chr22:42079636-42079763 | Common:1; Rare:37 | ||||
| chr22:42090681-42090953 | Common:2; Rare:120; Clinvar (pathogenic):1 | ||||
| chr22:42614850-42615246 | Common:3; Rare:164 | ||||
| chr22:42649311-42649485 | Common:1; Rare:69 | ||||
| chr22:43089321-43089496 | Common:3; Rare:58 | ||||
| chr22:43812230-43812441 | Common:3; Rare:71 |