| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:176361762-176361890 | Rare:34 | ||||
| chr5:176388555-176388802 | Common:4; Rare:91 | ||||
| chr5:176448196-176448410 | Common:1; Rare:75 | ||||
| chr5:176537912-176538116 | Common:1; Rare:67 | ||||
| chr5:177006667-177006860 | Common:1; Rare:65 | ||||
| chr5:177022612-177022741 | Rare:50 | ||||
| chr5:177133412-177133853 | Rare:156 | ||||
| chr5:177351643-177351977 | Rare:83 | ||||
| chr5:177509800-177509874 | Common:1; Rare:31 | ||||
| chr5:177510323-177510487 | Common:2; Rare:40 | ||||
| chr5:177516887-177517093 | Common:2; Rare:81; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:178627005-178627234 | Common:6; Rare:79 | ||||
| chr5:179550539-179550858 | Rare:148 | ||||
| chr5:179698590-179699065 | Common:3; Rare:169 | ||||
| chr5:179806321-179806447 | Rare:40 |