| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41688810-41688997 | Rare:75 | ||||
| chr22:41800483-41800746 | Common:1; Rare:89 | ||||
| chr22:41832909-41833184 | Common:3; Rare:93 | ||||
| chr22:41833205-41833944 | Common:4; Rare:245 | ||||
| chr22:41946704-41946958 | Common:3; Rare:64 | ||||
| chr22:41947058-41947177 | Common:1; Rare:43 | ||||
| chr22:41976350-41976590 | Common:1; Rare:42 | ||||
| chr22:41976610-41977070 | Rare:119 | ||||
| chr22:41977340-41977690 | Common:2; Rare:55 | ||||
| chr22:42070771-42071064 | Common:3; Rare:66 | ||||
| chr22:42079340-42079850 | Common:5; Rare:134 | ||||
| chr22:42079870-42080160 | Rare:96 | ||||
| chr22:42090675-42090963 | Common:2; Rare:127; Clinvar (pathogenic):1 | ||||
| chr22:42343330-42343790 | Common:2; Rare:126 | ||||
| chr22:42519764-42519961 | Common:1; Rare:77 |