| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:16616958-16617233 | Common:2; Rare:78; Clinvar (benign):6 | ||||
| chr5:16936231-16936447 | Common:3; Rare:59 | ||||
| chr5:31532052-31532332 | Common:3; Rare:76 | ||||
| chr5:31854790-31855110 | Common:2; Rare:113 | ||||
| chr5:32098280-32098480 | Rare:57; Clinvar:1 | ||||
| chr5:32174247-32174379 | Common:1; Rare:52 | ||||
| chr5:32710581-32710713 | Common:1; Rare:32 | ||||
| chr5:32712261-32712318 | Rare:15 | ||||
| chr5:33440606-33441112 | Common:7; Rare:141 | ||||
| chr5:34008027-34008214 | Common:2; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34656087-34656474 | Common:4; Rare:107 | ||||
| chr5:34839264-34839393 | Common:2; Rare:39 | ||||
| chr5:34915487-34915741 | Common:1; Rare:57 | ||||
| chr5:36151839-36152174 | Rare:96 | ||||
| chr5:36606450-36606631 | Rare:34 |