| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177431585-177431744 | Common:2; Rare:34 | ||||
| chr5:177497553-177497870 | Common:1; Rare:116 | ||||
| chr5:177509548-177509955 | Common:3; Rare:148 | ||||
| chr5:177510671-177510948 | Common:3; Rare:61 | ||||
| chr5:177516925-177517079 | Rare:55; Clinvar (pathogenic):1 | ||||
| chr5:177553375-177553399 | Rare:1 | ||||
| chr5:177592376-177592673 | Common:1; Rare:87 | ||||
| chr5:178204339-178204584 | Common:4; Rare:99 | ||||
| chr5:178231023-178231257 | Common:1; Rare:58 | ||||
| chr5:178231430-178231726 | Common:3; Rare:141 | ||||
| chr5:179550812-179550874 | Rare:26 | ||||
| chr5:179618533-179618702 | Rare:28 | ||||
| chr5:179820733-179820922 | Common:4; Rare:71; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:179822781-179822813 | Rare:6 | ||||
| chr5:180802768-180803023 | Common:8; Rare:94 |