| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:73578539-73578827 | Common:9; Rare:96 | ||||
| chr7:73683416-73683631 | Common:3; Rare:89 | ||||
| chr7:74254366-74254523 | Rare:71 | ||||
| chr7:74289305-74289476 | Common:3; Rare:74 | ||||
| chr7:76047774-76048176 | Common:2; Rare:116 | ||||
| chr7:76302520-76303069 | Common:3; Rare:231; Clinvar:17; Clinvar (benign):13; Clinvar (pathogenic):5 | ||||
| chr7:77122287-77122638 | Common:2; Rare:72 | ||||
| chr7:77696214-77696495 | Rare:120 | ||||
| chr7:77696694-77697051 | Rare:153 | ||||
| chr7:77798312-77798937 | Common:1; Rare:149 | ||||
| chr7:79452653-79452941 | Common:1; Rare:49 | ||||
| chr7:79453566-79453763 | Common:1; Rare:52 | ||||
| chr7:79453832-79454133 | Common:1; Rare:75 | ||||
| chr7:84194709-84194841 | Common:1; Rare:13 | ||||
| chr7:87152294-87152493 | Common:2; Rare:68 |