| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:128965448-128965590 | Common:2; Rare:39 | ||||
| chr5:131170708-131171013 | Common:1; Rare:62; Clinvar (benign):2 | ||||
| chr5:131385313-131385637 | Rare:61 | ||||
| chr5:131635143-131635416 | Common:1; Rare:104 | ||||
| chr5:131796936-131797248 | Rare:91 | ||||
| chr5:132257475-132257732 | Common:8; Rare:67 | ||||
| chr5:132294087-132294430 | Common:1; Rare:83 | ||||
| chr5:132369595-132369785 | Common:4; Rare:56; Clinvar (benign):1 | ||||
| chr5:132410603-132411041 | Common:2; Rare:92 | ||||
| chr5:132490743-132491055 | Rare:81 | ||||
| chr5:132557204-132557255 | Rare:15 | ||||
| chr5:132777117-132777359 | Common:3; Rare:58 | ||||
| chr5:132866457-132866981 | Common:4; Rare:167; Clinvar:3; Clinvar (benign):3 | ||||
| chr5:132963499-132963834 | Common:1; Rare:83 | ||||
| chr5:132963909-132964021 | Rare:42 |