| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138033002-138033180 | Common:1; Rare:63 | ||||
| chr5:138338018-138338118 | Rare:38 | ||||
| chr5:138338203-138338283 | Common:1; Rare:36 | ||||
| chr5:138464947-138465229 | Common:1; Rare:69 | ||||
| chr5:138465820-138466045 | Rare:104 | ||||
| chr5:138543017-138543512 | Common:3; Rare:146 | ||||
| chr5:138557403-138557667 | Rare:64 | ||||
| chr5:138575244-138575498 | Common:1; Rare:124 | ||||
| chr5:138575595-138575729 | Rare:29 | ||||
| chr5:138753255-138753503 | Common:2; Rare:87 | ||||
| chr5:138886036-138886276 | Rare:53 | ||||
| chr5:138904167-138904420 | Common:1; Rare:55 | ||||
| chr5:139198277-139198528 | Rare:82; Clinvar (benign):1 | ||||
| chr5:139273880-139274150 | Common:1; Rare:116; Clinvar (benign):2 | ||||
| chr5:139341815-139341972 | Common:1; Rare:48 |