| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:124800625-124800823 | Common:1; Rare:40 | ||||
| chr11:124800824-124800908 | Common:1; Rare:13 | ||||
| chr11:124876034-124876197 | Rare:62; Clinvar:2 | ||||
| chr11:124876336-124876537 | Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:124876627-124876860 | Common:2; Rare:49 | ||||
| chr11:124953912-124954246 | Common:5; Rare:94 | ||||
| chr11:124954313-124954430 | Common:1; Rare:26 | ||||
| chr11:125062936-125063069 | Common:1; Rare:28 | ||||
| chr11:125063102-125063368 | Common:3; Rare:71 | ||||
| chr11:125111454-125112103 | Common:5; Rare:154 | ||||
| chr11:125569341-125569556 | Common:1; Rare:64 | ||||
| chr11:125591736-125591877 | Common:2; Rare:37 | ||||
| chr11:125592032-125592209 | Rare:33 | ||||
| chr11:125592286-125592951 | Common:6; Rare:209; Clinvar (benign):1 | ||||
| chr11:125593180-125593386 | Rare:39 |