| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138178935-138179201 | Common:3; Rare:53 | ||||
| chr5:138331777-138332151 | Common:2; Rare:88 | ||||
| chr5:138338001-138338296 | Common:2; Rare:122 | ||||
| chr5:138543095-138543585 | Common:2; Rare:159 | ||||
| chr5:138575326-138575718 | Common:2; Rare:144 | ||||
| chr5:138753271-138753507 | Common:2; Rare:80 | ||||
| chr5:139198289-139198538 | Rare:86; Clinvar (benign):1 | ||||
| chr5:139273945-139274142 | Rare:90 | ||||
| chr5:139293532-139293809 | Rare:89 | ||||
| chr5:139293906-139294012 | Rare:29 | ||||
| chr5:139341692-139341933 | Common:1; Rare:63 | ||||
| chr5:139404068-139404278 | Rare:58 | ||||
| chr5:139561137-139561358 | Common:1; Rare:90 | ||||
| chr5:140175017-140175232 | Rare:58 | ||||
| chr5:140303065-140303165 | Common:1; Rare:29 |