| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33439246-33440006 | Common:12; Rare:379 | ||||
| chr3:33440318-33440863 | Common:4; Rare:157 | ||||
| chr3:33441025-33441128 | Rare:26 | ||||
| chr3:33658927-33659632 | Common:7; Rare:194 | ||||
| chr3:33659634-33659786 | Common:1; Rare:38 | ||||
| chr3:33718179-33718374 | Rare:88 | ||||
| chr3:33798271-33799150 | Common:4; Rare:274 | ||||
| chr3:36993046-36993588 | Common:2; Rare:192; Clinvar:34; Clinvar (benign):15; Clinvar (pathogenic):4 | ||||
| chr3:37176319-37176677 | Common:1; Rare:101 | ||||
| chr3:37243137-37243271 | Common:2; Rare:37 | ||||
| chr3:37451952-37452159 | Common:1; Rare:60 | ||||
| chr3:37861600-37862000 | Common:1; Rare:109 | ||||
| chr3:37998997-37999217 | Common:3; Rare:67 | ||||
| chr3:38000846-38001246 | Common:4; Rare:106 | ||||
| chr3:38025120-38025325 | Common:3; Rare:49 |