| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40856598-40857154 | Common:2; Rare:212; Clinvar:3 | ||||
| chr22:40951136-40951396 | Common:2; Rare:86 | ||||
| chr22:41091456-41091823 | Common:6; Rare:126 | ||||
| chr22:41286164-41286533 | Common:2; Rare:114 | ||||
| chr22:41367193-41367502 | Rare:90 | ||||
| chr22:41446795-41446958 | Rare:65 | ||||
| chr22:41560884-41561139 | Common:9; Rare:72 | ||||
| chr22:41621017-41621368 | Common:7; Rare:131 | ||||
| chr22:41800506-41800631 | Rare:40 | ||||
| chr22:41832909-41833266 | Common:3; Rare:129 | ||||
| chr22:41899170-41899288 | Common:2; Rare:23 | ||||
| chr22:42070782-42071036 | Common:3; Rare:56 | ||||
| chr22:42074187-42074296 | Common:2; Rare:23 | ||||
| chr22:42079491-42079763 | Common:2; Rare:71 | ||||
| chr22:42090668-42091001 | Common:2; Rare:148; Clinvar (pathogenic):1 |