| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:127628940-127629241 | Common:1; Rare:101 | ||||
| chr3:128052137-128052515 | Common:4; Rare:129 | ||||
| chr3:128067279-128067559 | Rare:72 | ||||
| chr3:128123753-128124015 | Rare:70 | ||||
| chr3:128153324-128153581 | Common:2; Rare:73 | ||||
| chr3:128488492-128488640 | Common:1; Rare:34 | ||||
| chr3:128493193-128493385 | Rare:60 | ||||
| chr3:128681111-128681231 | Common:1; Rare:35 | ||||
| chr3:128879408-128879675 | Common:4; Rare:129; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129160982-129161152 | Common:1; Rare:66 | ||||
| chr3:129183806-129184075 | Common:2; Rare:91 | ||||
| chr3:129249503-129249675 | Common:3; Rare:51 | ||||
| chr3:129278761-129278900 | Common:4; Rare:43 | ||||
| chr3:129316242-129316315 | Rare:44 | ||||
| chr3:129439847-129440318 | Common:1; Rare:141; Clinvar:1; Clinvar (benign):1 |