| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:6009047-6009299 | Common:3; Rare:94; Clinvar:1; Clinvar (benign):7 | ||||
| chr7:6577396-6577579 | Rare:60 | ||||
| chr7:16645837-16646156 | Common:2; Rare:105 | ||||
| chr7:23105667-23105829 | Common:4; Rare:86; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:26200722-26201097 | Common:1; Rare:180 | ||||
| chr7:26201597-26201821 | Common:2; Rare:117 | ||||
| chr7:27185176-27185405 | Common:1; Rare:86 | ||||
| chr7:27740085-27740197 | Common:3; Rare:29 | ||||
| chr7:30594733-30595107 | Common:6; Rare:175; Clinvar:9; Clinvar (benign):14 | ||||
| chr7:39623469-39623717 | Rare:89 | ||||
| chr7:42932156-42932384 | Rare:84 | ||||
| chr7:44796401-44796686 | Common:2; Rare:99 | ||||
| chr7:44999886-45000201 | Common:1; Rare:65 | ||||
| chr7:48089025-48089265 | Common:3; Rare:60 | ||||
| chr7:56051429-56051837 | Common:1; Rare:154; Clinvar:5; Clinvar (benign):1 |