| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:35419274-35419412 | Common:1; Rare:36 | ||||
| chr11:35419555-35419605 | Rare:14 | ||||
| chr11:35943992-35944110 | Common:1; Rare:38 | ||||
| chr11:36289393-36289505 | Common:1; Rare:44 | ||||
| chr11:36510229-36510361 | Rare:40 | ||||
| chr11:40293159-40293316 | Common:1; Rare:31 | ||||
| chr11:41459455-41459533 | Common:1; Rare:16 | ||||
| chr11:41459567-41459706 | Common:1; Rare:25 | ||||
| chr11:41460102-41460155 | Rare:10 | ||||
| chr11:41460169-41460222 | Rare:10 | ||||
| chr11:43311727-43312053 | Common:2; Rare:105 | ||||
| chr11:43358839-43358983 | Rare:70 | ||||
| chr11:45804987-45805175 | Common:3; Rare:43; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:45847227-45847493 | Common:2; Rare:109 | ||||
| chr11:46120947-46121031 | Rare:8 |