| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179806900-179807101 | Common:3; Rare:66 | ||||
| chr5:179820713-179821039 | Common:6; Rare:127; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:179858797-179859047 | Rare:133 | ||||
| chr5:179907707-179908144 | Common:5; Rare:166 | ||||
| chr5:180071640-180071865 | Common:2; Rare:96 | ||||
| chr5:180291901-180292242 | Common:2; Rare:137 | ||||
| chr5:180353321-180353553 | Common:6; Rare:92 | ||||
| chr5:180802775-180802958 | Common:6; Rare:76 | ||||
| chr5:180803838-180804032 | Common:3; Rare:48 | ||||
| chr5:180809819-180809922 | Common:4; Rare:25 | ||||
| chr5:180810121-180810236 | Common:1; Rare:27 | ||||
| chr5:181040082-181040299 | Rare:43 | ||||
| chr5:181223118-181223313 | Rare:66 | ||||
| chr5:181223633-181223752 | Common:3; Rare:28 | ||||
| chr5:181224497-181224622 | Common:1; Rare:37 |