| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:32312895-32313371 | Common:3; Rare:134 | ||||
| chr5:32443761-32444523 | Common:11; Rare:330 | ||||
| chr5:32444641-32444792 | Rare:63 | ||||
| chr5:32531861-32532424 | Common:2; Rare:204 | ||||
| chr5:32585439-32585608 | Common:1; Rare:72 | ||||
| chr5:32709964-32710364 | Common:4; Rare:96 | ||||
| chr5:33440155-33440386 | Common:1; Rare:38 | ||||
| chr5:33440787-33441075 | Common:5; Rare:80 | ||||
| chr5:33441130-33441410 | Common:1; Rare:71 | ||||
| chr5:33891469-33891869 | Common:4; Rare:108 | ||||
| chr5:33891980-33892303 | Rare:76 | ||||
| chr5:33892380-33892770 | Common:2; Rare:86 | ||||
| chr5:34007992-34008380 | Common:4; Rare:121; Clinvar:2; Clinvar (benign):2 | ||||
| chr5:34656159-34656387 | Common:3; Rare:60 | ||||
| chr5:34656477-34657461 | Common:11; Rare:378 |