| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:77696198-77696475 | Common:1; Rare:108 | ||||
| chr7:77798353-77798910 | Common:1; Rare:136 | ||||
| chr7:79453589-79453689 | Rare:28 | ||||
| chr7:79453781-79454117 | Common:2; Rare:81 | ||||
| chr7:87152314-87152675 | Common:2; Rare:110 | ||||
| chr7:87193428-87193760 | Common:1; Rare:83 | ||||
| chr7:87345432-87345701 | Common:4; Rare:86 | ||||
| chr7:87876224-87876652 | Common:2; Rare:183 | ||||
| chr7:90154372-90154514 | Rare:39 | ||||
| chr7:90211628-90211946 | Common:4; Rare:98 | ||||
| chr7:90245083-90245243 | Rare:52 | ||||
| chr7:90346557-90346744 | Common:4; Rare:83 | ||||
| chr7:90596222-90596581 | Common:1; Rare:114 | ||||
| chr7:91880662-91880816 | Common:1; Rare:43 | ||||
| chr7:91940835-91941004 | Common:3; Rare:57; Clinvar:4; Clinvar (benign):1 |