| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:42090668-42090947 | Common:2; Rare:126; Clinvar (pathogenic):1 | ||||
| chr22:42614820-42615272 | Common:3; Rare:203 | ||||
| chr22:42649311-42649482 | Common:1; Rare:67 | ||||
| chr22:42720813-42720937 | Rare:39 | ||||
| chr22:42857167-42857430 | Common:3; Rare:108 | ||||
| chr22:43015087-43015384 | Common:2; Rare:121 | ||||
| chr22:43089325-43089496 | Common:3; Rare:55 | ||||
| chr22:43955303-43955571 | Common:3; Rare:82 | ||||
| chr22:44024214-44024359 | Common:1; Rare:53 | ||||
| chr22:45163766-45164003 | Common:2; Rare:92 | ||||
| chr22:45309692-45309983 | Common:1; Rare:115 | ||||
| chr22:45413594-45413716 | Rare:44 | ||||
| chr22:46053778-46053901 | Rare:43 | ||||
| chr22:46250254-46250528 | Common:3; Rare:90 | ||||
| chr22:46296745-46296922 | Rare:59 |