| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:75914902-75915164 | Common:3; Rare:89; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:75994614-75994786 | Common:3; Rare:87 | ||||
| chr7:76047943-76048157 | Common:1; Rare:72 | ||||
| chr7:76302849-76303066 | Rare:91; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr7:76303422-76303831 | Common:3; Rare:169; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:77696232-77696475 | Rare:99 | ||||
| chr7:77697072-77697150 | Common:1; Rare:25 | ||||
| chr7:77798374-77798857 | Common:1; Rare:115 | ||||
| chr7:87152270-87152493 | Common:2; Rare:80 | ||||
| chr7:87220526-87220682 | Common:1; Rare:45 | ||||
| chr7:87345461-87345701 | Common:4; Rare:81 | ||||
| chr7:87876131-87876681 | Common:3; Rare:217 | ||||
| chr7:88220022-88220151 | Rare:64 | ||||
| chr7:90346596-90346744 | Common:4; Rare:65 | ||||
| chr7:90403312-90403495 | Common:1; Rare:43 |