| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17013880-17013955 | Common:4; Rare:37 | ||||
| chr11:17014235-17014330 | Rare:34 | ||||
| chr11:17077608-17077857 | Common:2; Rare:104 | ||||
| chr11:17207911-17208111 | Common:2; Rare:75 | ||||
| chr11:17276541-17276832 | Common:5; Rare:82; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr11:17389290-17389481 | Common:2; Rare:37 | ||||
| chr11:18012903-18013251 | Common:6; Rare:116 | ||||
| chr11:18322119-18322337 | Common:5; Rare:87; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322437-18322626 | Common:2; Rare:74 | ||||
| chr11:18394421-18394667 | Common:1; Rare:98; Clinvar (benign):1 | ||||
| chr11:18396110-18396408 | Common:1; Rare:115 | ||||
| chr11:18526835-18526977 | Rare:70 | ||||
| chr11:18588667-18588941 | Common:4; Rare:86 | ||||
| chr11:18634313-18634566 | Common:2; Rare:81 | ||||
| chr11:18698661-18698820 | Common:4; Rare:41 |