| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177303655-177304053 | Common:4; Rare:155 | ||||
| chr5:177351643-177351968 | Rare:82 | ||||
| chr5:177497548-177497798 | Common:1; Rare:93 | ||||
| chr5:177516917-177517063 | Rare:56; Clinvar (pathogenic):1 | ||||
| chr5:178130823-178131039 | Rare:60 | ||||
| chr5:178941112-178941239 | Rare:33 | ||||
| chr5:179698603-179699100 | Common:4; Rare:178 | ||||
| chr5:179806304-179806456 | Rare:48 | ||||
| chr5:179806836-179807063 | Common:3; Rare:85 | ||||
| chr5:179821102-179821135 | Common:1; Rare:13; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:179858797-179859031 | Rare:123 | ||||
| chr5:180649521-180649709 | Rare:64 | ||||
| chr5:180802768-180802955 | Common:6; Rare:78 | ||||
| chr5:180810108-180810216 | Common:1; Rare:22 | ||||
| chr5:181223118-181223313 | Rare:66 |