| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17014251-17014330 | Rare:28 | ||||
| chr11:17077608-17077857 | Common:2; Rare:104 | ||||
| chr11:17207856-17208111 | Common:2; Rare:91 | ||||
| chr11:17276546-17276813 | Common:4; Rare:75; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:17351647-17352020 | Common:2; Rare:77 | ||||
| chr11:18012910-18013251 | Common:6; Rare:113 | ||||
| chr11:18106037-18106308 | Common:2; Rare:83 | ||||
| chr11:18248603-18248831 | Common:1; Rare:54 | ||||
| chr11:18266016-18266441 | Common:5; Rare:79 | ||||
| chr11:18266748-18266977 | Common:1; Rare:56 | ||||
| chr11:18322077-18322645 | Common:8; Rare:204; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18394372-18394633 | Common:1; Rare:109; Clinvar (benign):1 | ||||
| chr11:18526812-18527033 | Common:2; Rare:105 | ||||
| chr11:18588661-18588884 | Common:2; Rare:78 | ||||
| chr11:18634213-18634596 | Common:3; Rare:135 |