| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138178935-138179186 | Common:3; Rare:51 | ||||
| chr5:138331777-138332122 | Common:2; Rare:83 | ||||
| chr5:138337918-138338102 | Common:1; Rare:55 | ||||
| chr5:138338235-138338296 | Common:2; Rare:37 | ||||
| chr5:138543088-138543518 | Common:2; Rare:130 | ||||
| chr5:138575296-138575483 | Common:1; Rare:98 | ||||
| chr5:138753288-138753503 | Common:2; Rare:71 | ||||
| chr5:138875233-138875450 | Rare:38; Clinvar (benign):1 | ||||
| chr5:139198277-139198579 | Common:1; Rare:100; Clinvar (benign):1 | ||||
| chr5:139273950-139274162 | Rare:97 | ||||
| chr5:139341738-139341933 | Common:1; Rare:52 | ||||
| chr5:139404050-139404272 | Rare:68 | ||||
| chr5:139439453-139439582 | Common:1; Rare:38 | ||||
| chr5:139482288-139482461 | Rare:28 | ||||
| chr5:139561097-139561563 | Common:1; Rare:193 |