| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:39399656-39399796 | Common:3; Rare:57 | ||||
| chr22:40346434-40346556 | Rare:52; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:40819321-40819515 | Common:11; Rare:100 | ||||
| chr22:40856921-40857114 | Common:1; Rare:68; Clinvar:1 | ||||
| chr22:40951018-40951404 | Common:2; Rare:134 | ||||
| chr22:41286122-41286237 | Rare:43 | ||||
| chr22:41446785-41446958 | Rare:70 | ||||
| chr22:41468618-41468813 | Common:2; Rare:52 | ||||
| chr22:41468939-41469158 | Rare:66 | ||||
| chr22:41620981-41621370 | Common:7; Rare:140 | ||||
| chr22:41800489-41800694 | Common:1; Rare:70 | ||||
| chr22:41832840-41833137 | Common:3; Rare:94 | ||||
| chr22:41947093-41947199 | Rare:40 | ||||
| chr22:42079634-42079763 | Common:1; Rare:38 | ||||
| chr22:42090714-42090966 | Common:2; Rare:101; Clinvar (pathogenic):1 |