| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67634764-67635085 | Common:2; Rare:106 | ||||
| chr11:67645044-67645369 | Common:1; Rare:109 | ||||
| chr11:67805311-67805618 | Common:3; Rare:107 | ||||
| chr11:67884303-67884475 | Rare:49 | ||||
| chr11:67884852-67885005 | Common:1; Rare:47 | ||||
| chr11:67886346-67886553 | Common:2; Rare:45 | ||||
| chr11:68053969-68054260 | Rare:93 | ||||
| chr11:68343877-68344086 | Rare:58 | ||||
| chr11:68397177-68397286 | Rare:29 | ||||
| chr11:68812229-68812482 | Common:1; Rare:55; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:69479800-69479972 | Common:1; Rare:40 | ||||
| chr11:70410712-70411002 | Common:2; Rare:55 | ||||
| chr11:71723446-71723728 | Common:5; Rare:63 | ||||
| chr11:71745772-71745954 | Common:4; Rare:56 | ||||
| chr11:72004713-72004914 | Rare:59 |