| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:108498057-108498549 | Common:11; Rare:262 | ||||
| chr11:108593460-108593771 | Common:4; Rare:185 | ||||
| chr11:108664777-108665166 | Common:12; Rare:299 | ||||
| chr11:110092580-110093130 | Common:9; Rare:333 | ||||
| chr11:110093744-110093908 | Common:4; Rare:43 | ||||
| chr11:110296295-110297140 | Common:7; Rare:663; Clinvar:24 | ||||
| chr11:110429892-110430024 | Common:1; Rare:38 | ||||
| chr11:110430020-110430197 | Common:6; Rare:87 | ||||
| chr11:111602207-111602587 | Common:3; Rare:278 | ||||
| chr11:111766330-111766530 | Common:4; Rare:201 | ||||
| chr11:111766580-111766940 | Rare:132 | ||||
| chr11:111870730-111871060 | Common:4; Rare:66 | ||||
| chr11:111871184-111871409 | Common:1; Rare:70; Clinvar:1 | ||||
| chr11:111871470-111871790 | Rare:134; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:111878720-111878990 | Common:4; Rare:118 |