| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40346410-40346556 | Common:1; Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:40856590-40857126 | Common:2; Rare:198; Clinvar:1 | ||||
| chr22:41468997-41469159 | Rare:56 | ||||
| chr22:41621000-41621360 | Common:7; Rare:134 | ||||
| chr22:41800524-41800626 | Rare:32 | ||||
| chr22:41832809-41833137 | Common:3; Rare:100 | ||||
| chr22:42070802-42071003 | Common:3; Rare:44 | ||||
| chr22:42090730-42090945 | Common:1; Rare:79; Clinvar (pathogenic):1 | ||||
| chr22:42614940-42615245 | Common:3; Rare:125 | ||||
| chr22:42649311-42649479 | Common:1; Rare:65 | ||||
| chr22:43015086-43015384 | Common:2; Rare:122 | ||||
| chr22:43955303-43955580 | Common:3; Rare:84 | ||||
| chr22:44752465-44752613 | Common:4; Rare:54 | ||||
| chr22:45163777-45164003 | Common:2; Rare:82 | ||||
| chr22:46250282-46250361 | Common:1; Rare:22 |