| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177351643-177351958 | Rare:81 | ||||
| chr5:177367048-177367325 | Common:2; Rare:65 | ||||
| chr5:177473508-177473806 | Common:1; Rare:104 | ||||
| chr5:177483934-177484122 | Rare:59 | ||||
| chr5:177497540-177497868 | Common:1; Rare:120 | ||||
| chr5:177516875-177517093 | Common:2; Rare:88; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:178130868-178131026 | Rare:42 | ||||
| chr5:178153768-178154110 | Rare:105; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:178204326-178204534 | Common:3; Rare:73 | ||||
| chr5:178232551-178232843 | Common:3; Rare:90 | ||||
| chr5:178627012-178627298 | Common:8; Rare:95 | ||||
| chr5:178941081-178941242 | Common:1; Rare:42 | ||||
| chr5:179060249-179060388 | Common:1; Rare:40 | ||||
| chr5:179559559-179559814 | Common:1; Rare:74 | ||||
| chr5:179623609-179623983 | Common:4; Rare:134 |