| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:178130868-178131109 | Common:1; Rare:63 | ||||
| chr5:178153557-178153992 | Common:1; Rare:170; Clinvar:10; Clinvar (benign):5 | ||||
| chr5:178204320-178204555 | Common:3; Rare:85 | ||||
| chr5:178860024-178860114 | Common:2; Rare:22 | ||||
| chr5:179060234-179060464 | Common:2; Rare:62 | ||||
| chr5:179550454-179550858 | Common:4; Rare:178 | ||||
| chr5:179559559-179559814 | Common:1; Rare:74 | ||||
| chr5:179623368-179623989 | Common:4; Rare:224 | ||||
| chr5:179698293-179698422 | Common:1; Rare:33 | ||||
| chr5:179698575-179699099 | Common:4; Rare:186 | ||||
| chr5:179793887-179794048 | Common:1; Rare:38 | ||||
| chr5:179806845-179807070 | Common:3; Rare:85 | ||||
| chr5:179820702-179821141 | Common:7; Rare:158; Clinvar:9; Clinvar (benign):4 | ||||
| chr5:179858792-179859020 | Rare:118 | ||||
| chr5:180291925-180292239 | Common:2; Rare:126 |