| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138575231-138575497 | Common:1; Rare:126 | ||||
| chr5:138575660-138575963 | Rare:84 | ||||
| chr5:138753270-138753503 | Common:2; Rare:80 | ||||
| chr5:139198277-139198531 | Rare:83; Clinvar (benign):1 | ||||
| chr5:139273942-139274164 | Rare:102 | ||||
| chr5:139293519-139294019 | Rare:157 | ||||
| chr5:139294463-139294543 | Rare:40 | ||||
| chr5:139341701-139341969 | Common:1; Rare:73 | ||||
| chr5:139342207-139342493 | Common:3; Rare:105 | ||||
| chr5:139404050-139404330 | Common:1; Rare:79 | ||||
| chr5:139439453-139439594 | Common:1; Rare:39 | ||||
| chr5:139561088-139561600 | Common:1; Rare:210 | ||||
| chr5:139561723-139561812 | Rare:36 | ||||
| chr5:139659174-139659359 | Rare:44 | ||||
| chr5:140043237-140043417 | Common:1; Rare:44 |