| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:172983693-172983962 | Common:1; Rare:97 | ||||
| chr5:176388512-176388806 | Common:4; Rare:115 | ||||
| chr5:176389042-176389196 | Rare:39 | ||||
| chr5:176448216-176448427 | Common:1; Rare:80 | ||||
| chr5:176537820-176538063 | Rare:63 | ||||
| chr5:177022635-177022756 | Rare:46 | ||||
| chr5:177303632-177303962 | Common:4; Rare:135 | ||||
| chr5:177467255-177467632 | Common:1; Rare:115 | ||||
| chr5:177516863-177517069 | Common:2; Rare:86; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:177554544-177554652 | Common:2; Rare:37 | ||||
| chr5:177592137-177592282 | Common:2; Rare:74 | ||||
| chr5:178153855-178154107 | Rare:64; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:178231086-178231257 | Rare:42 | ||||
| chr5:178859794-178860026 | Common:2; Rare:73 | ||||
| chr5:179618024-179618267 | Common:1; Rare:79 |