| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128879421-128879675 | Common:4; Rare:124; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129183814-129184079 | Common:2; Rare:89 | ||||
| chr3:129278736-129278882 | Common:4; Rare:46 | ||||
| chr3:129439916-129440340 | Common:1; Rare:130; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129560485-129560646 | Rare:27 | ||||
| chr3:130893905-130894246 | Common:3; Rare:99 | ||||
| chr3:131026738-131026955 | Common:2; Rare:57 | ||||
| chr3:133661793-133662024 | Rare:54 | ||||
| chr3:134485402-134485772 | Rare:90 | ||||
| chr3:134485971-134486253 | Common:3; Rare:96 | ||||
| chr3:136818993-136819183 | Common:4; Rare:102 | ||||
| chr3:136862022-136862275 | Common:1; Rare:72 | ||||
| chr3:138115594-138115730 | Common:3; Rare:33 | ||||
| chr3:138348370-138348692 | Common:2; Rare:83 | ||||
| chr3:138594198-138594451 | Rare:75 |