| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18322397-18322619 | Common:2; Rare:78 | ||||
| chr11:18394401-18394633 | Common:1; Rare:92; Clinvar (benign):1 | ||||
| chr11:18526803-18527063 | Common:3; Rare:119 | ||||
| chr11:18588667-18588815 | Rare:53 | ||||
| chr11:18634245-18634594 | Common:3; Rare:124 | ||||
| chr11:18698533-18698747 | Common:3; Rare:49 | ||||
| chr11:22625808-22626002 | Common:2; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:26994028-26994162 | Common:1; Rare:20 | ||||
| chr11:27363069-27363377 | Rare:138 | ||||
| chr11:27506752-27506864 | Common:1; Rare:47 | ||||
| chr11:28108096-28108421 | Common:1; Rare:96 | ||||
| chr11:30322944-30323169 | Common:1; Rare:65 | ||||
| chr11:31369724-31369887 | Rare:50 | ||||
| chr11:31509575-31509790 | Common:1; Rare:67 | ||||
| chr11:32583663-32583906 | Rare:91 |