| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:131165164-131165391 | Common:2; Rare:92; Clinvar (benign):1 | ||||
| chr5:131170693-131171002 | Common:1; Rare:63; Clinvar (benign):1 | ||||
| chr5:131252949-131253065 | Common:1; Rare:26 | ||||
| chr5:131263889-131264123 | Common:1; Rare:89 | ||||
| chr5:131635117-131635446 | Common:1; Rare:120 | ||||
| chr5:131635584-131635726 | Rare:39 | ||||
| chr5:131796928-131797282 | Rare:99 | ||||
| chr5:132257475-132257745 | Common:8; Rare:72 | ||||
| chr5:132294102-132294441 | Common:1; Rare:80 | ||||
| chr5:132369575-132369820 | Common:4; Rare:75; Clinvar (benign):1 | ||||
| chr5:132370144-132370195 | Rare:18; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr5:132387662-132387818 | Common:1; Rare:29 | ||||
| chr5:132410603-132411010 | Common:1; Rare:82 | ||||
| chr5:132489459-132489597 | Rare:29 | ||||
| chr5:132490717-132491093 | Common:2; Rare:99 |