| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:14664587-14664950 | Common:3; Rare:140 | ||||
| chr5:16465716-16465915 | Common:1; Rare:39 | ||||
| chr5:31532002-31532395 | Common:4; Rare:110 | ||||
| chr5:32174218-32174421 | Common:1; Rare:75 | ||||
| chr5:32585435-32585624 | Common:2; Rare:82 | ||||
| chr5:32710581-32710733 | Common:1; Rare:38 | ||||
| chr5:32711167-32711340 | Rare:29 | ||||
| chr5:33440605-33441134 | Common:7; Rare:148 | ||||
| chr5:34007997-34008354 | Common:3; Rare:120; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34656150-34656480 | Common:3; Rare:82 | ||||
| chr5:34915218-34915355 | Rare:38 | ||||
| chr5:34915478-34915750 | Common:1; Rare:68 | ||||
| chr5:35047824-35048306 | Common:4; Rare:113 | ||||
| chr5:35617688-35617928 | Common:1; Rare:49 | ||||
| chr5:36151801-36152195 | Rare:109 |