| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177133453-177133800 | Rare:123 | ||||
| chr5:177134147-177134193 | Rare:8 | ||||
| chr5:177303678-177304076 | Common:3; Rare:148 | ||||
| chr5:177367034-177367325 | Common:2; Rare:71 | ||||
| chr5:177483890-177484191 | Rare:90 | ||||
| chr5:177497540-177497887 | Common:1; Rare:124 | ||||
| chr5:177516932-177517084 | Rare:52; Clinvar (pathogenic):1 | ||||
| chr5:178006594-178006904 | Common:2; Rare:20 | ||||
| chr5:178130848-178131039 | Rare:52 | ||||
| chr5:178153801-178154170 | Rare:101; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:178940990-178941241 | Common:1; Rare:68 | ||||
| chr5:179559543-179559805 | Common:1; Rare:74 | ||||
| chr5:179623599-179623983 | Common:4; Rare:136 | ||||
| chr5:179698580-179699099 | Common:4; Rare:184 | ||||
| chr5:179806900-179807070 | Common:3; Rare:58 |