| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40951056-40951460 | Common:2; Rare:135 | ||||
| chr22:40951559-40951716 | Common:2; Rare:49 | ||||
| chr22:41091478-41091827 | Common:6; Rare:124 | ||||
| chr22:41286134-41286446 | Common:2; Rare:103 | ||||
| chr22:41446784-41446979 | Rare:83 | ||||
| chr22:41468997-41469170 | Rare:65 | ||||
| chr22:41621018-41621368 | Common:7; Rare:131 | ||||
| chr22:41621746-41622083 | Common:1; Rare:81 | ||||
| chr22:41752370-41752605 | Common:1; Rare:54 | ||||
| chr22:41781090-41781434 | Common:2; Rare:92 | ||||
| chr22:41800517-41800702 | Common:1; Rare:58 | ||||
| chr22:41832656-41832723 | Rare:12 | ||||
| chr22:41832831-41833306 | Common:3; Rare:162 | ||||
| chr22:41926326-41926473 | Rare:36; Clinvar (benign):1 | ||||
| chr22:41940129-41940473 | Common:2; Rare:68 |