| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:24644752-24645042 | Common:3; Rare:65 | ||||
| chr5:31532032-31532381 | Common:3; Rare:100 | ||||
| chr5:32174267-32174442 | Common:2; Rare:63 | ||||
| chr5:32531089-32531203 | Rare:25 | ||||
| chr5:32531481-32531936 | Common:2; Rare:79 | ||||
| chr5:32585442-32585624 | Common:2; Rare:78 | ||||
| chr5:32709859-32710211 | Common:1; Rare:59 | ||||
| chr5:32710554-32710768 | Common:1; Rare:51 | ||||
| chr5:32711099-32711349 | Rare:39 | ||||
| chr5:33440606-33440788 | Common:1; Rare:43 | ||||
| chr5:33440802-33441134 | Common:5; Rare:97 | ||||
| chr5:33441199-33441421 | Common:1; Rare:52 | ||||
| chr5:34008015-34008222 | Common:2; Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34656159-34656473 | Common:3; Rare:79 | ||||
| chr5:34839267-34839398 | Common:2; Rare:40 |