| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:172896765-172897084 | Common:1; Rare:55 | ||||
| chr5:172900084-172900208 | Common:1; Rare:24 | ||||
| chr5:172903149-172903195 | Rare:7 | ||||
| chr5:177282337-177282579 | Rare:41; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr5:177619144-177619188 | Rare:6 | ||||
| chr5:177672213-177672352 | Common:5; Rare:20 | ||||
| chr5:178206580-178206843 | Common:2; Rare:81 | ||||
| chr5:178213886-178213916 | Rare:6 | ||||
| chr5:178228860-178229027 | Common:1; Rare:39 | ||||
| chr5:179530721-179530829 | Rare:28 | ||||
| chr5:179829178-179829368 | Common:1; Rare:39 | ||||
| chr5:180590205-180590448 | Common:3; Rare:58 | ||||
| chr5:180830902-180831055 | Common:1; Rare:39 | ||||
| chr5:180831567-180831679 | Common:2; Rare:47 | ||||
| chr5:180834559-180834792 | Rare:45 |