| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177303678-177304051 | Common:3; Rare:143 | ||||
| chr5:177497540-177497723 | Rare:74 | ||||
| chr5:177516887-177517084 | Common:2; Rare:77; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:178204223-178204534 | Common:5; Rare:112 | ||||
| chr5:178222123-178222412 | Rare:71 | ||||
| chr5:178941101-178941244 | Rare:35 | ||||
| chr5:179550501-179550563 | Common:2; Rare:24 | ||||
| chr5:179559559-179559781 | Common:1; Rare:62 | ||||
| chr5:179596350-179596611 | Rare:74 | ||||
| chr5:179698575-179699091 | Common:4; Rare:182 | ||||
| chr5:179820704-179820926 | Common:6; Rare:81; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:179823843-179824322 | Common:1; Rare:197; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr5:179858792-179859062 | Rare:143 | ||||
| chr5:180802775-180802980 | Common:8; Rare:80 | ||||
| chr5:180810108-180810219 | Common:1; Rare:25 |