| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:137889312-137889457 | Common:1; Rare:50 | ||||
| chr5:138033021-138033210 | Common:1; Rare:67 | ||||
| chr5:138178597-138178776 | Rare:43 | ||||
| chr5:138178953-138179178 | Common:2; Rare:47 | ||||
| chr5:138331777-138332056 | Common:2; Rare:67 | ||||
| chr5:138338203-138338283 | Common:1; Rare:36 | ||||
| chr5:138543095-138543542 | Common:2; Rare:140 | ||||
| chr5:138558551-138558768 | Common:1; Rare:56; Clinvar:1 | ||||
| chr5:138575269-138575729 | Common:2; Rare:175 | ||||
| chr5:138753277-138753507 | Common:2; Rare:77 | ||||
| chr5:138875302-138875461 | Rare:28; Clinvar (benign):1 | ||||
| chr5:139198284-139198531 | Rare:83; Clinvar (benign):1 | ||||
| chr5:139273953-139274121 | Rare:75 | ||||
| chr5:139404069-139404270 | Rare:56 | ||||
| chr5:139526465-139526555 | Common:1; Rare:28 |