| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34051417-34051805 | Rare:133 | ||||
| chr11:34052030-34052457 | Common:5; Rare:189 | ||||
| chr11:34053364-34053558 | Rare:49 | ||||
| chr11:34105365-34105799 | Common:4; Rare:131 | ||||
| chr11:34357945-34358410 | Common:3; Rare:124 | ||||
| chr11:34438623-34439060 | Common:3; Rare:137; Clinvar (benign):1 | ||||
| chr11:34439092-34439286 | Common:3; Rare:58 | ||||
| chr11:34439372-34439497 | Rare:23 | ||||
| chr11:34915720-34915798 | Common:2; Rare:15 | ||||
| chr11:34916006-34916432 | Common:7; Rare:152; Clinvar:3; Clinvar (benign):6 | ||||
| chr11:34916484-34916720 | Common:7; Rare:95; Clinvar:4; Clinvar (benign):8 | ||||
| chr11:35138830-35139279 | Common:2; Rare:109 | ||||
| chr11:35139604-35139759 | Common:2; Rare:40 | ||||
| chr11:35618164-35618478 | Common:5; Rare:89 | ||||
| chr11:35619263-35619291 | Rare:14 |