| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177303678-177303868 | Common:3; Rare:93 | ||||
| chr5:177462380-177462555 | Common:1; Rare:36 | ||||
| chr5:177497575-177497771 | Common:1; Rare:71 | ||||
| chr5:177516875-177517093 | Common:2; Rare:88; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:177525142-177525453 | Rare:71 | ||||
| chr5:178113364-178113671 | Common:4; Rare:97 | ||||
| chr5:178130887-178131039 | Rare:40 | ||||
| chr5:178204258-178204537 | Common:5; Rare:100 | ||||
| chr5:178230903-178231233 | Common:2; Rare:78 | ||||
| chr5:178231340-178231499 | Rare:60 | ||||
| chr5:178232536-178232902 | Common:4; Rare:123 | ||||
| chr5:178895844-178895937 | Rare:34 | ||||
| chr5:178940969-178941239 | Common:1; Rare:73 | ||||
| chr5:179023676-179023867 | Common:2; Rare:60 | ||||
| chr5:179060206-179060485 | Common:2; Rare:75 |