| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18322086-18322345 | Common:6; Rare:100; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322476-18322629 | Common:2; Rare:63 | ||||
| chr11:18394380-18394630 | Common:1; Rare:102; Clinvar (benign):1 | ||||
| chr11:18526841-18526987 | Rare:72 | ||||
| chr11:18588661-18588905 | Common:2; Rare:85 | ||||
| chr11:18698635-18698772 | Common:2; Rare:41 | ||||
| chr11:20363551-20363788 | Common:5; Rare:46 | ||||
| chr11:20364087-20364197 | Rare:24 | ||||
| chr11:22625808-22626002 | Common:2; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:27506738-27506864 | Common:1; Rare:53 | ||||
| chr11:28108142-28108414 | Common:1; Rare:78 | ||||
| chr11:30016968-30017058 | Rare:24 | ||||
| chr11:30322828-30323137 | Common:2; Rare:79 | ||||
| chr11:31369737-31369882 | Rare:45 | ||||
| chr11:31509576-31509794 | Common:1; Rare:69 |