| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49007106-49007463 | Common:2; Rare:145 | ||||
| chr3:49018549-49018611 | Rare:22 | ||||
| chr3:49021502-49021765 | Rare:60; Clinvar:1 | ||||
| chr3:49022011-49022211 | Rare:72; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49024946-49025272 | Rare:90 | ||||
| chr3:49029264-49029482 | Common:1; Rare:127 | ||||
| chr3:49093922-49094314 | Rare:94 | ||||
| chr3:49100112-49100214 | Rare:35; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:49104708-49104887 | Rare:78; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:49120785-49121121 | Rare:91 | ||||
| chr3:49132944-49133114 | Rare:33; Clinvar:2 | ||||
| chr3:49339930-49340110 | Common:2; Rare:85 | ||||
| chr3:49358946-49359227 | Rare:51 | ||||
| chr3:49411894-49412448 | Common:2; Rare:203 | ||||
| chr3:49469895-49470386 | Common:2; Rare:152 |