| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:127628942-127629286 | Common:1; Rare:111 | ||||
| chr3:127672808-127673028 | Common:4; Rare:106 | ||||
| chr3:127915197-127915340 | Rare:38 | ||||
| chr3:128052128-128052562 | Common:4; Rare:146 | ||||
| chr3:128123690-128124045 | Rare:103 | ||||
| chr3:128153365-128153505 | Rare:41 | ||||
| chr3:128487914-128488074 | Common:1; Rare:41 | ||||
| chr3:128493195-128493385 | Rare:60 | ||||
| chr3:128650238-128650332 | Common:2; Rare:20 | ||||
| chr3:128650560-128650936 | Common:2; Rare:153 | ||||
| chr3:128725981-128726225 | Common:1; Rare:73; Clinvar:3 | ||||
| chr3:128879357-128879835 | Common:5; Rare:223; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr3:128994063-128994222 | Common:1; Rare:53 | ||||
| chr3:129121640-129121943 | Common:1; Rare:57 | ||||
| chr3:129122117-129122326 | Common:1; Rare:24 |