| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:176388503-176388781 | Common:1; Rare:103 | ||||
| chr5:176448185-176448413 | Common:1; Rare:79 | ||||
| chr5:177006702-177006880 | Common:2; Rare:60 | ||||
| chr5:177022591-177022741 | Common:1; Rare:60 | ||||
| chr5:177303655-177303811 | Common:4; Rare:72 | ||||
| chr5:177473539-177473665 | Rare:44 | ||||
| chr5:177497553-177497860 | Common:1; Rare:115 | ||||
| chr5:177516887-177517065 | Common:2; Rare:73; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:177592255-177592379 | Common:1; Rare:59; Clinvar:1 | ||||
| chr5:178859807-178859980 | Common:1; Rare:50 | ||||
| chr5:179023692-179023843 | Common:1; Rare:43 | ||||
| chr5:179617569-179617908 | Rare:85 | ||||
| chr5:179618024-179618254 | Common:1; Rare:76 | ||||
| chr5:179698613-179699105 | Common:4; Rare:172 | ||||
| chr5:179806808-179807018 | Common:3; Rare:83 |