| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:120336157-120336440 | Rare:118 | ||||
| chr11:123062062-123062663 | Common:9; Rare:270 | ||||
| chr11:124673710-124673929 | Common:4; Rare:68 | ||||
| chr11:124762244-124762405 | Rare:44 | ||||
| chr11:124800406-124800475 | Rare:27 | ||||
| chr11:124954031-124954149 | Common:3; Rare:30 | ||||
| chr11:125592506-125592913 | Common:6; Rare:131 | ||||
| chr11:125625875-125625935 | Rare:23 | ||||
| chr11:126211634-126211819 | Rare:84 | ||||
| chr11:126268763-126269198 | Common:1; Rare:168; Clinvar:2; Clinvar (benign):3 | ||||
| chr11:126303967-126304093 | Rare:75 | ||||
| chr11:128693958-128694161 | Rare:37 | ||||
| chr11:130314381-130314517 | Common:1; Rare:45 | ||||
| chr11:130448445-130448662 | Rare:53 | ||||
| chr11:134068779-134069078 | Common:2; Rare:107 |