| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179806265-179806448 | Rare:54 | ||||
| chr5:179806817-179807097 | Common:3; Rare:100 | ||||
| chr5:179820686-179821073 | Common:6; Rare:137; Clinvar:6; Clinvar (benign):2 | ||||
| chr5:179858765-179859025 | Rare:138 | ||||
| chr5:179871460-179871737 | Common:2; Rare:62 | ||||
| chr5:180291909-180292197 | Common:2; Rare:105 | ||||
| chr5:180353321-180353505 | Common:5; Rare:75 | ||||
| chr5:180494169-180494396 | Common:2; Rare:73 | ||||
| chr5:180649571-180649699 | Rare:48 | ||||
| chr5:180802756-180802953 | Common:6; Rare:82 | ||||
| chr5:180809813-180809932 | Common:4; Rare:26 | ||||
| chr5:180810108-180810281 | Common:5; Rare:52 | ||||
| chr5:180861150-180861619 | Common:4; Rare:153 | ||||
| chr5:180988680-180988973 | Common:2; Rare:29 | ||||
| chr5:181223122-181223313 | Rare:65 |