| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:176721113-176721282 | Common:2; Rare:31 | ||||
| chr5:176772658-176772854 | Common:2; Rare:40 | ||||
| chr5:177267429-177267633 | Common:1; Rare:45; Clinvar (benign):1 | ||||
| chr5:177611168-177611311 | Rare:28 | ||||
| chr5:177616462-177616692 | Rare:33 | ||||
| chr5:177618289-177618548 | Common:2; Rare:44 | ||||
| chr5:177619116-177619216 | Rare:16 | ||||
| chr5:177632042-177632095 | Rare:10 | ||||
| chr5:177672224-177672395 | Common:3; Rare:22 | ||||
| chr5:177689145-177689385 | Common:5; Rare:59 | ||||
| chr5:177725061-177725352 | Common:5; Rare:24 | ||||
| chr5:177807432-177807738 | Common:5; Rare:12 | ||||
| chr5:177875470-177875728 | Common:1; Rare:5 | ||||
| chr5:177939458-177939656 | Common:1; Rare:40 | ||||
| chr5:178187356-178187502 | Common:3; Rare:26 |