| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:131263909-131264139 | Rare:87 | ||||
| chr5:131635109-131635432 | Common:1; Rare:117 | ||||
| chr5:131635443-131635723 | Rare:80 | ||||
| chr5:131796909-131797221 | Rare:89 | ||||
| chr5:132294092-132294400 | Common:1; Rare:73 | ||||
| chr5:132369575-132369759 | Common:3; Rare:57 | ||||
| chr5:132369882-132369947 | Common:2; Rare:22; Clinvar:2; Clinvar (benign):2 | ||||
| chr5:132370147-132370210 | Rare:24; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr5:132410603-132410956 | Common:1; Rare:68 | ||||
| chr5:132490771-132491020 | Rare:64 | ||||
| chr5:132556872-132557249 | Rare:134; Clinvar:1 | ||||
| chr5:132866457-132866711 | Common:2; Rare:83; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963260-132963392 | Rare:31 | ||||
| chr5:132963499-132963737 | Rare:64 | ||||
| chr5:133051851-133052351 | Common:1; Rare:161 |