| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:128083294-128083400 | Rare:29 | ||||
| chr5:128083596-128083766 | Common:2; Rare:70 | ||||
| chr5:129094518-129094769 | Common:2; Rare:105 | ||||
| chr5:131165194-131165484 | Common:2; Rare:118; Clinvar (benign):1 | ||||
| chr5:131170679-131171002 | Common:1; Rare:70; Clinvar (benign):1 | ||||
| chr5:131635141-131635312 | Rare:75 | ||||
| chr5:131796970-131797202 | Rare:66 | ||||
| chr5:132369575-132369964 | Common:8; Rare:129; Clinvar:6; Clinvar (benign):6 | ||||
| chr5:132556784-132557026 | Common:1; Rare:82; Clinvar:1 | ||||
| chr5:132737506-132737676 | Rare:50 | ||||
| chr5:132830602-132830781 | Rare:48 | ||||
| chr5:132866363-132866698 | Common:1; Rare:104; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963503-132963699 | Rare:54 | ||||
| chr5:133051852-133052306 | Common:1; Rare:149 | ||||
| chr5:133968551-133968718 | Rare:70 |