| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18588667-18588815 | Rare:53 | ||||
| chr11:18634332-18634566 | Common:2; Rare:74 | ||||
| chr11:18698547-18698747 | Common:3; Rare:46 | ||||
| chr11:18791691-18791869 | Rare:64 | ||||
| chr11:20669465-20669641 | Common:2; Rare:81 | ||||
| chr11:22338278-22338421 | Rare:29 | ||||
| chr11:22625808-22626002 | Common:2; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:24496737-24497221 | Common:4; Rare:128 | ||||
| chr11:27506738-27506864 | Common:1; Rare:53 | ||||
| chr11:28108115-28108414 | Common:1; Rare:90 | ||||
| chr11:30016956-30017103 | Rare:41 | ||||
| chr11:30322944-30323176 | Common:1; Rare:68 | ||||
| chr11:31369728-31369882 | Rare:47 | ||||
| chr11:31509575-31509922 | Common:1; Rare:126 | ||||
| chr11:31811299-31811492 | Rare:29 |