| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177303678-177304051 | Common:3; Rare:143 | ||||
| chr5:177497584-177497856 | Common:1; Rare:97 | ||||
| chr5:177516906-177517100 | Common:1; Rare:71; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:178130869-178131039 | Rare:44 | ||||
| chr5:178153828-178154176 | Rare:94; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:178940966-178941242 | Common:1; Rare:73 | ||||
| chr5:179550523-179550569 | Common:2; Rare:10 | ||||
| chr5:179559559-179559793 | Common:1; Rare:67 | ||||
| chr5:179698575-179699091 | Common:4; Rare:182 | ||||
| chr5:179806304-179806448 | Rare:44 | ||||
| chr5:179806900-179807035 | Common:3; Rare:46 | ||||
| chr5:179820713-179821018 | Common:6; Rare:118; Clinvar:2; Clinvar (benign):2 | ||||
| chr5:179823969-179824230 | Common:1; Rare:107; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr5:179858792-179859025 | Rare:122 | ||||
| chr5:180071698-180071855 | Common:1; Rare:70 |