| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:179071463-179071947 | Common:2; Rare:317 | ||||
| chr3:179072058-179072630 | Common:5; Rare:167 | ||||
| chr3:179147810-179148421 | Common:36; Rare:644 | ||||
| chr3:179148420-179149590 | Common:9; Rare:650; Clinvar (benign):2 | ||||
| chr3:179259816-179260859 | Common:16; Rare:437 | ||||
| chr3:179322733-179323601 | Common:30; Rare:773 | ||||
| chr3:179323620-179324099 | Common:16; Rare:391 | ||||
| chr3:179324489-179324889 | Common:3; Rare:99 | ||||
| chr3:179347550-179347829 | Common:8; Rare:352 | ||||
| chr3:179347783-179348183 | Common:2; Rare:146 | ||||
| chr3:179348169-179349053 | Common:9; Rare:272 | ||||
| chr3:179376471-179376871 | Common:6; Rare:84 | ||||
| chr3:179450808-179451208 | Common:1; Rare:190 | ||||
| chr3:179451178-179451325 | Common:1; Rare:30 | ||||
| chr3:179451320-179451970 | Common:7; Rare:517 |