| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18322039-18322370 | Common:6; Rare:117; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322385-18322653 | Common:2; Rare:93 | ||||
| chr11:18394319-18394806 | Common:3; Rare:171; Clinvar (benign):1 | ||||
| chr11:18395990-18396395 | Common:3; Rare:131 | ||||
| chr11:18526516-18526752 | Common:2; Rare:58 | ||||
| chr11:18526766-18527073 | Common:3; Rare:130 | ||||
| chr11:18527165-18527304 | Rare:25 | ||||
| chr11:18588570-18588900 | Common:2; Rare:116 | ||||
| chr11:18634282-18634652 | Common:5; Rare:130 | ||||
| chr11:18634728-18634920 | Common:2; Rare:49 | ||||
| chr11:18698539-18698804 | Common:6; Rare:68 | ||||
| chr11:18706411-18706524 | Rare:21 | ||||
| chr11:19116888-19117265 | Common:3; Rare:104 | ||||
| chr11:19117483-19117616 | Rare:23 | ||||
| chr11:19240457-19240483 | Common:1; Rare:3 |