| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:130893898-130894231 | Common:3; Rare:99 | ||||
| chr3:131381479-131381801 | Common:2; Rare:80 | ||||
| chr3:131502814-131503056 | Common:1; Rare:99 | ||||
| chr3:132659785-132659928 | Common:3; Rare:32 | ||||
| chr3:133038170-133038418 | Common:1; Rare:84 | ||||
| chr3:133661767-133661968 | Rare:45 | ||||
| chr3:134374437-134374627 | Rare:56 | ||||
| chr3:134485402-134485766 | Rare:87 | ||||
| chr3:134485957-134486258 | Common:3; Rare:106 | ||||
| chr3:136250260-136250381 | Common:2; Rare:47; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:136752341-136752667 | Common:1; Rare:106 | ||||
| chr3:136819069-136819177 | Common:3; Rare:74 | ||||
| chr3:136862016-136862275 | Common:1; Rare:77 | ||||
| chr3:138115601-138115706 | Common:2; Rare:25 | ||||
| chr3:138174848-138174960 | Common:1; Rare:25 |