| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:76302866-76302996 | Rare:62; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr7:76303691-76303847 | Common:1; Rare:72; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):6 | ||||
| chr7:77696198-77696460 | Common:1; Rare:98 | ||||
| chr7:77798351-77798910 | Common:1; Rare:136 | ||||
| chr7:79453532-79453639 | Rare:27 | ||||
| chr7:79453938-79454044 | Common:1; Rare:28 | ||||
| chr7:80134528-80134897 | Common:4; Rare:126 | ||||
| chr7:87152270-87152468 | Common:1; Rare:68 | ||||
| chr7:87345426-87345732 | Common:5; Rare:93 | ||||
| chr7:87876213-87876685 | Common:3; Rare:198 | ||||
| chr7:90346509-90346736 | Common:3; Rare:90 | ||||
| chr7:91880672-91880822 | Common:2; Rare:40 | ||||
| chr7:92134427-92134819 | Common:5; Rare:106 | ||||
| chr7:92246099-92246315 | Common:3; Rare:62 | ||||
| chr7:92528413-92528808 | Common:3; Rare:124; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):3 |