| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:128344404-128344688 | Rare:60; Clinvar:10; Clinvar (benign):2 | ||||
| chr5:129007161-129007437 | Common:2; Rare:41 | ||||
| chr5:130530176-130530442 | Common:2; Rare:56 | ||||
| chr5:131159622-131159779 | Common:1; Rare:25 | ||||
| chr5:131286168-131286383 | Common:1; Rare:22 | ||||
| chr5:131368283-131368444 | Rare:33 | ||||
| chr5:131658466-131658581 | Rare:22 | ||||
| chr5:131712594-131712938 | Rare:52 | ||||
| chr5:131768241-131768463 | Rare:38 | ||||
| chr5:132271746-132272114 | Common:3; Rare:140 | ||||
| chr5:132346991-132347124 | Common:1; Rare:21 | ||||
| chr5:132362740-132362796 | Rare:11 | ||||
| chr5:132363486-132363691 | Common:2; Rare:41 | ||||
| chr5:133090485-133090841 | Common:4; Rare:63 | ||||
| chr5:133103854-133104448 | Common:2; Rare:151 |