| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:131796936-131797203 | Rare:79 | ||||
| chr5:132294117-132294453 | Common:1; Rare:79 | ||||
| chr5:132410734-132410995 | Rare:53 | ||||
| chr5:132490761-132491020 | Rare:68 | ||||
| chr5:132777188-132777359 | Common:1; Rare:42 | ||||
| chr5:132866435-132866694 | Common:1; Rare:84; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:133026517-133026777 | Common:5; Rare:61 | ||||
| chr5:133051862-133052361 | Common:1; Rare:157 | ||||
| chr5:133968554-133968737 | Rare:73 | ||||
| chr5:134004516-134004855 | Common:2; Rare:115 | ||||
| chr5:134004928-134005046 | Rare:25 | ||||
| chr5:134226025-134226413 | Common:1; Rare:124 | ||||
| chr5:134371031-134371167 | Common:1; Rare:35 | ||||
| chr5:134371175-134371520 | Common:2; Rare:104 | ||||
| chr5:134411846-134412008 | Rare:56 |