| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177133453-177133800 | Rare:123 | ||||
| chr5:177303678-177304043 | Common:3; Rare:141 | ||||
| chr5:177516932-177517068 | Rare:48; Clinvar (pathogenic):1 | ||||
| chr5:177600021-177600159 | Common:3; Rare:43 | ||||
| chr5:178859857-178860000 | Rare:39 | ||||
| chr5:178940966-178941233 | Common:1; Rare:71 | ||||
| chr5:179023683-179023812 | Common:2; Rare:36 | ||||
| chr5:179559560-179559776 | Common:1; Rare:62 | ||||
| chr5:179698610-179699092 | Common:4; Rare:170 | ||||
| chr5:179793800-179794054 | Common:1; Rare:60 | ||||
| chr5:179821115-179821141 | Common:1; Rare:10; Clinvar:2; Clinvar (benign):2 | ||||
| chr5:179858797-179858989 | Rare:107 | ||||
| chr5:180291909-180292191 | Common:2; Rare:102 | ||||
| chr5:180802792-180802956 | Common:6; Rare:71 | ||||
| chr5:180861223-180861405 | Common:2; Rare:72 |