| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:43869447-43869657 | Rare:68 | ||||
| chr7:43926373-43926478 | Rare:33 | ||||
| chr7:44044584-44044740 | Common:2; Rare:44 | ||||
| chr7:44123509-44123753 | Common:4; Rare:70 | ||||
| chr7:44490566-44490708 | Common:1; Rare:56 | ||||
| chr7:44573866-44574053 | Common:3; Rare:58 | ||||
| chr7:44582164-44582499 | Common:1; Rare:131 | ||||
| chr7:44606459-44606631 | Common:1; Rare:59 | ||||
| chr7:44796375-44796791 | Common:3; Rare:161 | ||||
| chr7:45111665-45111799 | Common:1; Rare:50 | ||||
| chr7:56051396-56051845 | Common:1; Rare:169; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56106395-56106535 | Common:6; Rare:62 | ||||
| chr7:64563063-64563274 | Common:3; Rare:52 | ||||
| chr7:66114807-66114927 | Common:1; Rare:54 | ||||
| chr7:66115179-66115353 | Rare:40 |