| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46846225-46846409 | Rare:49 | ||||
| chr11:47176849-47177105 | Common:1; Rare:104 | ||||
| chr11:47214843-47215110 | Common:2; Rare:69; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47269991-47270184 | Common:1; Rare:66 | ||||
| chr11:47565540-47565634 | Common:2; Rare:15 | ||||
| chr11:47578947-47579094 | Rare:76; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642461-47642724 | Rare:105 | ||||
| chr11:57324890-57325173 | Common:1; Rare:87 | ||||
| chr11:57530699-57530852 | Common:1; Rare:37 | ||||
| chr11:57567589-57567756 | Rare:58 | ||||
| chr11:57597558-57597720 | Rare:39; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:57657522-57657797 | Common:4; Rare:69 | ||||
| chr11:57712204-57712618 | Common:9; Rare:133 | ||||
| chr11:57741255-57741598 | Common:1; Rare:130 | ||||
| chr11:58578101-58578179 | Rare:23 |