| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177553730-177554260 | Common:3; Rare:187 | ||||
| chr5:177554524-177554684 | Common:3; Rare:57 | ||||
| chr5:177599979-177600251 | Common:8; Rare:158; Clinvar:1; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr5:178113371-178113562 | Common:4; Rare:120 | ||||
| chr5:178130410-178130720 | Common:2; Rare:129 | ||||
| chr5:178130819-178131114 | Common:3; Rare:123 | ||||
| chr5:178153737-178154151 | Rare:229; Clinvar:10; Clinvar (benign):3 | ||||
| chr5:178204326-178205007 | Common:12; Rare:419 | ||||
| chr5:178232173-178232858 | Common:14; Rare:359 | ||||
| chr5:178626938-178627242 | Common:14; Rare:178 | ||||
| chr5:178730586-178730883 | Common:4; Rare:104 | ||||
| chr5:178859560-178860130 | Common:9; Rare:206 | ||||
| chr5:178895551-178896065 | Common:10; Rare:253 | ||||
| chr5:179023704-179023844 | Common:1; Rare:38 | ||||
| chr5:179550454-179550600 | Common:4; Rare:54 |