| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:178204241-178204534 | Common:5; Rare:107 | ||||
| chr5:178222123-178222286 | Rare:26 | ||||
| chr5:178895815-178895946 | Rare:52 | ||||
| chr5:179023674-179023878 | Common:2; Rare:64 | ||||
| chr5:179550528-179550572 | Common:2; Rare:10 | ||||
| chr5:179550796-179550858 | Rare:22 | ||||
| chr5:179623599-179623770 | Common:1; Rare:80 | ||||
| chr5:179698580-179699099 | Common:4; Rare:184 | ||||
| chr5:179806310-179806400 | Rare:26 | ||||
| chr5:179806895-179807063 | Common:3; Rare:59 | ||||
| chr5:179820703-179821141 | Common:7; Rare:158; Clinvar:9; Clinvar (benign):4 | ||||
| chr5:179858797-179859031 | Rare:123 | ||||
| chr5:179907714-179908018 | Common:2; Rare:126 | ||||
| chr5:180802756-180802976 | Common:8; Rare:86 | ||||
| chr5:180803777-180803948 | Common:1; Rare:38 |