| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:13277378-13277660 | Common:2; Rare:81 | ||||
| chr11:13463098-13463403 | Common:1; Rare:110 | ||||
| chr11:14358774-14359008 | Rare:52 | ||||
| chr11:14511408-14511744 | Common:2; Rare:57 | ||||
| chr11:14517722-14517939 | Common:1; Rare:58 | ||||
| chr11:14520273-14520502 | Rare:75 | ||||
| chr11:16738466-16738873 | Common:3; Rare:100 | ||||
| chr11:17077616-17077868 | Common:2; Rare:104 | ||||
| chr11:17207858-17208240 | Common:2; Rare:126 | ||||
| chr11:18322101-18322352 | Common:6; Rare:95; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322450-18322737 | Common:2; Rare:100 | ||||
| chr11:18341285-18341560 | Rare:83 | ||||
| chr11:18394405-18394629 | Common:1; Rare:90; Clinvar (benign):1 | ||||
| chr11:18526801-18526997 | Common:1; Rare:90 | ||||
| chr11:18588616-18588952 | Common:4; Rare:108 |