| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:176448162-176448409 | Common:1; Rare:86 | ||||
| chr5:176537921-176538127 | Common:1; Rare:71 | ||||
| chr5:177006548-177006828 | Common:3; Rare:84 | ||||
| chr5:177022610-177022741 | Rare:52 | ||||
| chr5:177133474-177133800 | Rare:117 | ||||
| chr5:177303683-177303958 | Common:3; Rare:116 | ||||
| chr5:177367030-177367363 | Common:2; Rare:80 | ||||
| chr5:177497575-177497861 | Common:1; Rare:104 | ||||
| chr5:177516901-177517068 | Common:2; Rare:66; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:177592006-177592295 | Common:2; Rare:115; Clinvar:1 | ||||
| chr5:178113386-178113681 | Common:3; Rare:94 | ||||
| chr5:178130823-178131039 | Rare:60 | ||||
| chr5:178153751-178154103 | Rare:112; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:178204339-178204548 | Common:3; Rare:74 | ||||
| chr5:179023791-179023834 | Rare:10 |