| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177467255-177467631 | Common:1; Rare:114 | ||||
| chr5:177473571-177474035 | Common:2; Rare:113 | ||||
| chr5:177496782-177496967 | Rare:46 | ||||
| chr5:177497552-177497860 | Common:1; Rare:115 | ||||
| chr5:177516598-177517100 | Common:5; Rare:193; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr5:177554539-177554681 | Common:2; Rare:46 | ||||
| chr5:177592114-177592317 | Common:2; Rare:105; Clinvar:1 | ||||
| chr5:178113343-178113751 | Common:6; Rare:128 | ||||
| chr5:178130643-178130743 | Rare:22 | ||||
| chr5:178130763-178131122 | Common:2; Rare:101 | ||||
| chr5:178131293-178131665 | Common:3; Rare:80 | ||||
| chr5:178153768-178153815 | Rare:15 | ||||
| chr5:178153851-178154125 | Rare:68; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:178204326-178204812 | Common:6; Rare:168 | ||||
| chr5:178232727-178232859 | Common:2; Rare:54 |