| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:76201572-76201935 | Common:3; Rare:74 | ||||
| chr7:76303619-76303825 | Common:1; Rare:90; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:76358723-76359136 | Common:1; Rare:149 | ||||
| chr7:76359338-76359462 | Common:6; Rare:46 | ||||
| chr7:76627242-76627390 | Common:5; Rare:44 | ||||
| chr7:77122136-77122671 | Common:3; Rare:112 | ||||
| chr7:77537634-77538078 | Common:5; Rare:168 | ||||
| chr7:77696133-77696484 | Common:1; Rare:133 | ||||
| chr7:77696757-77697003 | Rare:109 | ||||
| chr7:77697055-77697191 | Common:2; Rare:40 | ||||
| chr7:77798353-77798986 | Common:1; Rare:150 | ||||
| chr7:78770882-78771422 | Rare:103 | ||||
| chr7:79453559-79453755 | Common:1; Rare:49 | ||||
| chr7:79453760-79454089 | Common:2; Rare:79 | ||||
| chr7:80918351-80918512 | Rare:25 |