| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33391507-33391885 | Common:3; Rare:94 | ||||
| chr6:33410901-33411069 | Rare:34 | ||||
| chr6:33414324-33414539 | Common:2; Rare:48 | ||||
| chr6:33417856-33418009 | Rare:64 | ||||
| chr6:33418015-33418456 | Common:2; Rare:106 | ||||
| chr6:33454393-33454612 | Rare:63 | ||||
| chr6:34236752-34236906 | Common:2; Rare:63 | ||||
| chr6:34248450-34248581 | Rare:22 | ||||
| chr6:34392262-34392670 | Rare:155 | ||||
| chr6:34426010-34426173 | Common:4; Rare:71; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:34696374-34696431 | Common:1; Rare:17 | ||||
| chr6:34696448-34696574 | Rare:30 | ||||
| chr6:34696709-34697012 | Common:1; Rare:69 | ||||
| chr6:34757379-34757554 | Rare:54 | ||||
| chr6:34887928-34888124 | Common:1; Rare:53 |