| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34052119-34052378 | Common:2; Rare:115 | ||||
| chr11:34105490-34105753 | Common:2; Rare:86 | ||||
| chr11:34916287-34916676 | Common:10; Rare:158; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35943969-35944103 | Common:2; Rare:44 | ||||
| chr11:36510229-36510372 | Rare:43 | ||||
| chr11:43358815-43358983 | Rare:80 | ||||
| chr11:44066094-44066359 | Common:3; Rare:69 | ||||
| chr11:44565281-44565701 | Common:3; Rare:104 | ||||
| chr11:45803937-45804049 | Common:1; Rare:22 | ||||
| chr11:45804258-45804484 | Common:1; Rare:46 | ||||
| chr11:45804965-45805193 | Common:3; Rare:59; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:45805321-45805764 | Common:2; Rare:81; Clinvar:5; Clinvar (benign):2 | ||||
| chr11:45847144-45847535 | Common:2; Rare:156 | ||||
| chr11:46120945-46121317 | Common:2; Rare:59 | ||||
| chr11:46617144-46617600 | Common:5; Rare:129 |