| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177516932-177517079 | Rare:51; Clinvar (pathogenic):1 | ||||
| chr5:178006786-178006904 | Common:1; Rare:15 | ||||
| chr5:178130882-178131039 | Rare:42 | ||||
| chr5:178153828-178154092 | Rare:78; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:178204258-178204534 | Common:5; Rare:100 | ||||
| chr5:178205679-178205978 | Common:1; Rare:84 | ||||
| chr5:178232201-178232482 | Common:6; Rare:133 | ||||
| chr5:178626984-178627239 | Common:7; Rare:91 | ||||
| chr5:178941010-178941239 | Common:1; Rare:63 | ||||
| chr5:179559560-179559805 | Common:1; Rare:72 | ||||
| chr5:179624362-179624449 | Rare:21 | ||||
| chr5:179698603-179699099 | Common:4; Rare:178 | ||||
| chr5:179806310-179806417 | Rare:31 | ||||
| chr5:179820713-179820969 | Common:6; Rare:104; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:179858797-179859025 | Rare:119 |