| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:134226033-134226407 | Common:1; Rare:121 | ||||
| chr5:134371031-134371184 | Common:1; Rare:39 | ||||
| chr5:134411846-134412008 | Rare:56 | ||||
| chr5:134524172-134524380 | Common:2; Rare:49 | ||||
| chr5:134648662-134648822 | Rare:45 | ||||
| chr5:135399073-135399325 | Rare:66 | ||||
| chr5:135578926-135579196 | Common:2; Rare:77 | ||||
| chr5:136060659-136060935 | Common:3; Rare:52; Clinvar (pathogenic):1 | ||||
| chr5:136132755-136132936 | Common:1; Rare:54 | ||||
| chr5:137753870-137754078 | Rare:38 | ||||
| chr5:137880335-137880641 | Common:1; Rare:46 | ||||
| chr5:137889312-137889457 | Common:1; Rare:50 | ||||
| chr5:138033025-138033177 | Common:1; Rare:53 | ||||
| chr5:138338012-138338272 | Common:1; Rare:104 | ||||
| chr5:138543095-138543518 | Common:2; Rare:129 |