| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177022635-177022741 | Rare:39 | ||||
| chr5:177303700-177304048 | Common:3; Rare:135 | ||||
| chr5:177351643-177351962 | Rare:81 | ||||
| chr5:177516925-177517098 | Rare:60; Clinvar (pathogenic):1 | ||||
| chr5:179559511-179559814 | Common:1; Rare:93 | ||||
| chr5:179623616-179623940 | Common:4; Rare:126 | ||||
| chr5:179698580-179699092 | Common:4; Rare:180 | ||||
| chr5:179806298-179806487 | Rare:64 | ||||
| chr5:179806817-179807070 | Common:3; Rare:93 | ||||
| chr5:179820749-179820907 | Common:2; Rare:56; Clinvar (benign):1 | ||||
| chr5:179823969-179824231 | Common:1; Rare:108; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr5:179858797-179859026 | Rare:120 | ||||
| chr5:179907796-179908015 | Common:2; Rare:106 | ||||
| chr5:180291925-180292191 | Common:2; Rare:99 | ||||
| chr5:180353321-180353512 | Common:5; Rare:78 |