| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:173917907-173918206 | Common:1; Rare:68 | ||||
| chr5:176361739-176361890 | Rare:44 | ||||
| chr5:176388555-176388822 | Common:4; Rare:107 | ||||
| chr5:176448162-176448410 | Common:1; Rare:86 | ||||
| chr5:177006427-177006489 | Rare:19 | ||||
| chr5:177022635-177022807 | Rare:65 | ||||
| chr5:177133453-177133885 | Rare:151 | ||||
| chr5:177288589-177288842 | Common:1; Rare:45; Clinvar (pathogenic):1 | ||||
| chr5:177303691-177303988 | Common:3; Rare:122 | ||||
| chr5:177367193-177367345 | Common:1; Rare:27 | ||||
| chr5:177483866-177484190 | Rare:96 | ||||
| chr5:177496782-177497085 | Common:3; Rare:69 | ||||
| chr5:177497529-177497863 | Common:1; Rare:122 | ||||
| chr5:177516887-177517100 | Common:2; Rare:81; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:177599843-177600155 | Common:3; Rare:85 |