| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:176388569-176388840 | Common:4; Rare:106 | ||||
| chr5:177022635-177022741 | Rare:39 | ||||
| chr5:177133453-177133853 | Rare:145 | ||||
| chr5:177303678-177303902 | Common:3; Rare:100 | ||||
| chr5:177497575-177497819 | Common:1; Rare:86 | ||||
| chr5:177516925-177517079 | Rare:55; Clinvar (pathogenic):1 | ||||
| chr5:179559560-179559771 | Common:1; Rare:60 | ||||
| chr5:179623624-179623988 | Common:4; Rare:132 | ||||
| chr5:179698681-179699095 | Common:3; Rare:135 | ||||
| chr5:179858798-179858993 | Rare:108 | ||||
| chr5:180353321-180353557 | Common:6; Rare:93 | ||||
| chr5:180810115-180810271 | Common:3; Rare:47 | ||||
| chr5:180861226-180861430 | Common:2; Rare:80 | ||||
| chr5:181223118-181223287 | Rare:57 | ||||
| chr5:181261081-181261286 | Rare:71 |