| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138331777-138332122 | Common:2; Rare:83 | ||||
| chr5:138338090-138338119 | Rare:14 | ||||
| chr5:138338203-138338277 | Common:1; Rare:33 | ||||
| chr5:138543110-138543522 | Common:2; Rare:128 | ||||
| chr5:138753268-138753503 | Common:2; Rare:81 | ||||
| chr5:139198284-139198549 | Rare:90; Clinvar (benign):1 | ||||
| chr5:139273950-139274158 | Rare:95 | ||||
| chr5:139341572-139341953 | Common:1; Rare:97 | ||||
| chr5:139439441-139439648 | Common:2; Rare:56 | ||||
| chr5:139561133-139561391 | Common:1; Rare:106 | ||||
| chr5:139561728-139561800 | Rare:30 | ||||
| chr5:140174989-140175208 | Rare:65 | ||||
| chr5:140303050-140303160 | Common:1; Rare:38 | ||||
| chr5:140557405-140557560 | Common:2; Rare:97 | ||||
| chr5:140564303-140564449 | Common:1; Rare:44 |