| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41544440-41544725 | Common:3; Rare:81 | ||||
| chr22:41560932-41561132 | Common:9; Rare:62 | ||||
| chr22:41621006-41621398 | Common:7; Rare:144 | ||||
| chr22:41800517-41800688 | Common:1; Rare:55 | ||||
| chr22:41832909-41833309 | Common:3; Rare:141 | ||||
| chr22:41998669-41998803 | Common:1; Rare:44 | ||||
| chr22:42070766-42070934 | Common:1; Rare:37 | ||||
| chr22:42079432-42079738 | Common:3; Rare:72 | ||||
| chr22:42090730-42091007 | Common:1; Rare:103; Clinvar (pathogenic):1 | ||||
| chr22:42614853-42615244 | Common:3; Rare:159 | ||||
| chr22:42649311-42649482 | Common:1; Rare:67 | ||||
| chr22:42857160-42857471 | Common:3; Rare:128 | ||||
| chr22:42876457-42876460 | Rare:1 | ||||
| chr22:43015063-43015384 | Common:2; Rare:128 | ||||
| chr22:43089332-43089491 | Common:3; Rare:51 |