| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66843597-66843764 | Common:1; Rare:72 | ||||
| chr11:66843813-66843865 | Rare:19 | ||||
| chr11:66856107-66856616 | Common:1; Rare:159 | ||||
| chr11:66856666-66857256 | Common:1; Rare:166 | ||||
| chr11:66857458-66857515 | Rare:9 | ||||
| chr11:66857608-66857822 | Common:3; Rare:55 | ||||
| chr11:66957797-66957880 | Rare:17 | ||||
| chr11:66958315-66958877 | Common:6; Rare:163; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:67056326-67056443 | Rare:15 | ||||
| chr11:67056599-67056977 | Common:1; Rare:95 | ||||
| chr11:67057078-67057285 | Rare:43 | ||||
| chr11:67118661-67119386 | Common:3; Rare:210 | ||||
| chr11:67119612-67119734 | Rare:33 | ||||
| chr11:67119921-67120125 | Rare:47 | ||||
| chr11:67120303-67120387 | Rare:19 |