| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:176448194-176448399 | Common:1; Rare:72 | ||||
| chr5:177022635-177022741 | Rare:39 | ||||
| chr5:177303683-177304008 | Common:3; Rare:129 | ||||
| chr5:177497552-177497863 | Common:1; Rare:115 | ||||
| chr5:177516932-177517084 | Rare:52; Clinvar (pathogenic):1 | ||||
| chr5:178153792-178154110 | Rare:95; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:178204339-178204533 | Common:3; Rare:68 | ||||
| chr5:178205679-178205978 | Common:1; Rare:84 | ||||
| chr5:178941010-178941256 | Common:1; Rare:66 | ||||
| chr5:179559560-179559803 | Common:1; Rare:71 | ||||
| chr5:179698681-179699099 | Common:3; Rare:138 | ||||
| chr5:179824066-179824323 | Common:1; Rare:98; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr5:179858792-179859020 | Rare:118 | ||||
| chr5:180353321-180353537 | Common:5; Rare:86 | ||||
| chr5:180802792-180802956 | Common:6; Rare:71 |