| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:122845516-122845625 | Common:3; Rare:43 | ||||
| chr5:123036458-123036574 | Rare:49 | ||||
| chr5:123036623-123036981 | Common:2; Rare:91 | ||||
| chr5:123089023-123089291 | Common:10; Rare:110 | ||||
| chr5:123511984-123512268 | Rare:77 | ||||
| chr5:126423333-126423594 | Rare:74 | ||||
| chr5:126595192-126595327 | Common:2; Rare:63; Clinvar:1; Clinvar (benign):7 | ||||
| chr5:126776931-126777175 | Common:1; Rare:95; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:127030529-127030749 | Common:2; Rare:48 | ||||
| chr5:127290765-127290844 | Rare:12 | ||||
| chr5:127517513-127517712 | Common:4; Rare:85 | ||||
| chr5:128083315-128083391 | Rare:20 | ||||
| chr5:128083600-128083766 | Common:2; Rare:68 | ||||
| chr5:131635160-131635424 | Common:1; Rare:101 | ||||
| chr5:131796908-131797215 | Rare:89 |