| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177303678-177304075 | Common:3; Rare:148 | ||||
| chr5:177497575-177497870 | Common:1; Rare:105 | ||||
| chr5:177516938-177517079 | Rare:47; Clinvar (pathogenic):1 | ||||
| chr5:177592182-177592242 | Rare:32 | ||||
| chr5:178232788-178232937 | Common:1; Rare:61 | ||||
| chr5:178940936-178941239 | Common:1; Rare:80 | ||||
| chr5:179550323-179550563 | Common:4; Rare:69 | ||||
| chr5:179619296-179619716 | Common:1; Rare:75 | ||||
| chr5:179698580-179698612 | Rare:10 | ||||
| chr5:179698676-179699065 | Common:2; Rare:126 | ||||
| chr5:179806310-179806380 | Rare:22 | ||||
| chr5:179820731-179821105 | Common:4; Rare:138; Clinvar:7; Clinvar (benign):2 | ||||
| chr5:179823969-179824323 | Common:1; Rare:143; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr5:179858797-179859047 | Rare:133 | ||||
| chr5:180353321-180353512 | Common:5; Rare:78 |