| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:31532392-31532638 | Common:2; Rare:66 | ||||
| chr3:32502775-32502924 | Rare:44 | ||||
| chr3:32570738-32570925 | Rare:87 | ||||
| chr3:33097098-33097277 | Common:2; Rare:61; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33277294-33277495 | Common:2; Rare:55 | ||||
| chr3:33440944-33441076 | Rare:24 | ||||
| chr3:33798520-33798686 | Common:2; Rare:60 | ||||
| chr3:33798997-33799120 | Rare:40 | ||||
| chr3:36993073-36993563 | Common:2; Rare:166; Clinvar:27; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:37243166-37243365 | Common:1; Rare:50 | ||||
| chr3:39051944-39052028 | Common:1; Rare:31 | ||||
| chr3:39107564-39107680 | Common:2; Rare:39 | ||||
| chr3:39383289-39383443 | Common:2; Rare:26; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383582-39383660 | Rare:17; Clinvar:1 | ||||
| chr3:39406614-39406776 | Common:2; Rare:62 |