| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65711869-65712025 | Rare:49 | ||||
| chr11:65720481-65720585 | Common:1; Rare:59 | ||||
| chr11:65860174-65860430 | Common:1; Rare:85 | ||||
| chr11:65873577-65873791 | Common:1; Rare:74 | ||||
| chr11:65888426-65888676 | Common:1; Rare:87 | ||||
| chr11:65890470-65890730 | Common:4; Rare:85 | ||||
| chr11:66002108-66002543 | Common:3; Rare:123; Clinvar:5; Clinvar (benign):3 | ||||
| chr11:66058062-66058327 | Rare:60 | ||||
| chr11:66257602-66257813 | Rare:58 | ||||
| chr11:66268394-66268673 | Common:3; Rare:84 | ||||
| chr11:66347579-66347869 | Common:5; Rare:68 | ||||
| chr11:66480232-66480444 | Common:1; Rare:55 | ||||
| chr11:66510551-66510671 | Common:1; Rare:51; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr11:66593036-66593209 | Common:1; Rare:61 | ||||
| chr11:66616396-66616676 | Common:2; Rare:86 |