| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33277313-33277476 | Common:1; Rare:41 | ||||
| chr3:33440368-33440527 | Common:1; Rare:43 | ||||
| chr3:33718050-33718314 | Rare:101 | ||||
| chr3:33798495-33798686 | Common:2; Rare:69 | ||||
| chr3:33798985-33799341 | Common:1; Rare:99 | ||||
| chr3:35639581-35639599 | Rare:1 | ||||
| chr3:36993057-36993595 | Common:2; Rare:191; Clinvar:37; Clinvar (benign):17; Clinvar (pathogenic):4 | ||||
| chr3:37176225-37176387 | Rare:52 | ||||
| chr3:37243047-37243377 | Common:4; Rare:89 | ||||
| chr3:38024470-38024667 | Common:1; Rare:76 | ||||
| chr3:38133585-38133869 | Rare:50 | ||||
| chr3:38137020-38137447 | Common:1; Rare:109 | ||||
| chr3:39051944-39052072 | Common:1; Rare:49 | ||||
| chr3:39107555-39107680 | Common:2; Rare:40 | ||||
| chr3:39153538-39153868 | Common:6; Rare:103 |