| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:25783371-25783646 | Common:2; Rare:92; Clinvar (benign):3 | ||||
| chr3:25789966-25790118 | Common:4; Rare:60 | ||||
| chr3:28348592-28348724 | Rare:29 | ||||
| chr3:28348773-28349185 | Common:3; Rare:131 | ||||
| chr3:29280837-29281423 | Common:15; Rare:114 | ||||
| chr3:31532394-31532662 | Common:4; Rare:75 | ||||
| chr3:31981634-31981780 | Rare:39 | ||||
| chr3:32570645-32570939 | Rare:134 | ||||
| chr3:33097087-33097272 | Common:1; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33277312-33277482 | Common:1; Rare:45 | ||||
| chr3:33798296-33798857 | Common:3; Rare:164 | ||||
| chr3:33798985-33799062 | Rare:29 | ||||
| chr3:36992630-36992943 | Common:1; Rare:99 | ||||
| chr3:36993074-36993557 | Common:2; Rare:164; Clinvar:26; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:37176241-37176393 | Rare:49 |