| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179820471-179820704 | Common:1; Rare:40 | ||||
| chr5:179820795-179821139 | Common:4; Rare:132; Clinvar:8; Clinvar (benign):4 | ||||
| chr5:179822776-179823052 | Common:1; Rare:96; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr5:179858792-179859052 | Rare:137 | ||||
| chr5:180071671-180071862 | Common:1; Rare:85 | ||||
| chr5:180291933-180292212 | Common:2; Rare:114 | ||||
| chr5:180353282-180353512 | Common:10; Rare:102 | ||||
| chr5:180629562-180630015 | Common:4; Rare:110; Clinvar (benign):4 | ||||
| chr5:180649519-180649718 | Rare:68 | ||||
| chr5:180802756-180802986 | Common:8; Rare:89 | ||||
| chr5:180803803-180803943 | Common:1; Rare:32 | ||||
| chr5:180809808-180809946 | Common:4; Rare:27 | ||||
| chr5:180810054-180810284 | Common:6; Rare:78 | ||||
| chr5:180815481-180815798 | Common:2; Rare:59 | ||||
| chr5:180860635-180860712 | Common:1; Rare:4 |