| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:178232551-178232702 | Common:2; Rare:42 | ||||
| chr5:178232763-178232890 | Common:2; Rare:53 | ||||
| chr5:178859883-178860114 | Common:3; Rare:65 | ||||
| chr5:178941109-178941239 | Rare:34 | ||||
| chr5:179023676-179023844 | Common:2; Rare:49 | ||||
| chr5:179550796-179550876 | Rare:31 | ||||
| chr5:179559560-179559814 | Common:1; Rare:74 | ||||
| chr5:179623599-179623976 | Common:4; Rare:134 | ||||
| chr5:179698575-179699099 | Common:4; Rare:186 | ||||
| chr5:179793975-179794050 | Common:1; Rare:24 | ||||
| chr5:179806278-179806448 | Rare:49 | ||||
| chr5:179806615-179806712 | Common:1; Rare:23 | ||||
| chr5:179806845-179807102 | Common:3; Rare:93 | ||||
| chr5:179820704-179821141 | Common:7; Rare:158; Clinvar:9; Clinvar (benign):4 | ||||
| chr5:179858772-179859047 | Rare:150 |