| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65084012-65084302 | Common:1; Rare:94 | ||||
| chr11:65181180-65181378 | Common:1; Rare:54 | ||||
| chr11:65314693-65314928 | Rare:78 | ||||
| chr11:65333630-65333881 | Common:1; Rare:111 | ||||
| chr11:65386507-65386684 | Rare:59 | ||||
| chr11:65570422-65570504 | Rare:39 | ||||
| chr11:65662842-65663021 | Common:1; Rare:46 | ||||
| chr11:65663194-65663491 | Common:3; Rare:74 | ||||
| chr11:65860177-65860447 | Common:1; Rare:87 | ||||
| chr11:65872688-65872961 | Common:2; Rare:71; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:65873544-65873791 | Common:3; Rare:80 | ||||
| chr11:65888398-65888668 | Common:1; Rare:94 | ||||
| chr11:65919863-65920177 | Rare:103 | ||||
| chr11:65961601-65961764 | Rare:52 | ||||
| chr11:66002086-66002777 | Common:4; Rare:190; Clinvar:8; Clinvar (benign):3 |