| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:128082963-128083372 | Common:8; Rare:127 | ||||
| chr5:129094472-129094876 | Common:3; Rare:177 | ||||
| chr5:131165153-131165407 | Common:2; Rare:105; Clinvar (benign):1 | ||||
| chr5:131170670-131171013 | Common:1; Rare:80; Clinvar (benign):2 | ||||
| chr5:131532971-131533130 | Common:1; Rare:24 | ||||
| chr5:131635183-131635455 | Common:1; Rare:105 | ||||
| chr5:131796943-131797221 | Rare:78 | ||||
| chr5:132369595-132369964 | Common:8; Rare:120; Clinvar:6; Clinvar (benign):6 | ||||
| chr5:132370147-132370310 | Common:2; Rare:70; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
| chr5:132556831-132557032 | Common:1; Rare:71; Clinvar:1 | ||||
| chr5:132737413-132737711 | Rare:105 | ||||
| chr5:132778001-132778187 | Rare:34 | ||||
| chr5:132866471-132866694 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:133026508-133026769 | Common:5; Rare:67 | ||||
| chr5:133051852-133052366 | Common:1; Rare:162 |