| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:12687396-12687660 | Common:5; Rare:81 | ||||
| chr7:15686667-15686738 | Common:1; Rare:18 | ||||
| chr7:16465736-16465945 | Rare:33 | ||||
| chr7:16645655-16646165 | Common:2; Rare:172 | ||||
| chr7:17298431-17298761 | Common:3; Rare:87 | ||||
| chr7:17940416-17940584 | Common:1; Rare:85 | ||||
| chr7:20217375-20217564 | Common:1; Rare:42 | ||||
| chr7:22822676-22822954 | Common:3; Rare:104 | ||||
| chr7:23105673-23105829 | Common:3; Rare:83; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181921-23182088 | Rare:72 | ||||
| chr7:23299193-23299361 | Common:2; Rare:80 | ||||
| chr7:23531793-23532105 | Common:2; Rare:122 | ||||
| chr7:24757409-24757719 | Common:1; Rare:79 | ||||
| chr7:24980114-24980377 | Common:6; Rare:107 | ||||
| chr7:25125230-25125644 | Rare:167; Clinvar:3 |