| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:28241439-28241672 | Common:1; Rare:79 | ||||
| chr3:28348644-28348711 | Rare:15 | ||||
| chr3:28348760-28349185 | Common:3; Rare:137 | ||||
| chr3:29281003-29281076 | Rare:10 | ||||
| chr3:31532380-31532638 | Common:2; Rare:71 | ||||
| chr3:31981634-31981780 | Rare:39 | ||||
| chr3:32106410-32106703 | Common:4; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32570738-32570919 | Rare:85 | ||||
| chr3:32685079-32685386 | Rare:91 | ||||
| chr3:33097097-33097277 | Common:2; Rare:61; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33277325-33277501 | Common:1; Rare:49 | ||||
| chr3:33798435-33798686 | Common:2; Rare:81 | ||||
| chr3:33798985-33799163 | Rare:56 | ||||
| chr3:36993117-36993550 | Common:2; Rare:133; Clinvar:26; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr3:37243166-37243505 | Common:1; Rare:87 |