| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:176537849-176538175 | Common:1; Rare:106 | ||||
| chr5:177006329-177006494 | Rare:48 | ||||
| chr5:177006556-177006850 | Common:3; Rare:87 | ||||
| chr5:177022566-177022909 | Common:1; Rare:122 | ||||
| chr5:177133448-177133853 | Rare:145 | ||||
| chr5:177133992-177134193 | Common:1; Rare:53 | ||||
| chr5:177303654-177304025 | Common:4; Rare:149 | ||||
| chr5:177312293-177312518 | Rare:68 | ||||
| chr5:177351623-177351775 | Rare:42 | ||||
| chr5:177351809-177352040 | Rare:58 | ||||
| chr5:177367038-177367390 | Common:2; Rare:94 | ||||
| chr5:177425932-177426066 | Rare:35 | ||||
| chr5:177496791-177497079 | Common:3; Rare:66 | ||||
| chr5:177497550-177497865 | Common:1; Rare:116 | ||||
| chr5:177516881-177517084 | Common:2; Rare:81; Clinvar:1; Clinvar (pathogenic):1 |