| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38570147-38570490 | Common:5; Rare:67 | ||||
| chr22:38656348-38656649 | Common:1; Rare:74 | ||||
| chr22:38681816-38682003 | Common:1; Rare:78 | ||||
| chr22:39349757-39349998 | Common:1; Rare:72 | ||||
| chr22:40177793-40177936 | Rare:38 | ||||
| chr22:40346434-40346556 | Rare:52; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:40819298-40819544 | Common:11; Rare:114 | ||||
| chr22:40856761-40857149 | Common:2; Rare:143; Clinvar:3 | ||||
| chr22:41468472-41468756 | Common:2; Rare:81 | ||||
| chr22:41469055-41469149 | Rare:39 | ||||
| chr22:41621005-41621370 | Common:7; Rare:135 | ||||
| chr22:41800542-41800631 | Rare:24 | ||||
| chr22:41832871-41833137 | Common:3; Rare:86 | ||||
| chr22:42090730-42090945 | Common:1; Rare:79; Clinvar (pathogenic):1 | ||||
| chr22:42614858-42615244 | Common:3; Rare:158 |