| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:76047950-76048220 | Common:2; Rare:94 | ||||
| chr7:76302581-76303073 | Common:3; Rare:217; Clinvar:17; Clinvar (benign):13; Clinvar (pathogenic):5 | ||||
| chr7:76303659-76303852 | Common:1; Rare:88; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):6 | ||||
| chr7:77122101-77122187 | Rare:17 | ||||
| chr7:77122302-77122647 | Common:2; Rare:71 | ||||
| chr7:77696132-77696475 | Common:1; Rare:127 | ||||
| chr7:77697042-77697164 | Common:1; Rare:44 | ||||
| chr7:77798330-77799002 | Common:1; Rare:162 | ||||
| chr7:79452766-79452855 | Rare:18 | ||||
| chr7:79452858-79453190 | Common:2; Rare:83; Clinvar (benign):2 | ||||
| chr7:79453555-79453689 | Rare:35 | ||||
| chr7:79453723-79454123 | Common:3; Rare:99 | ||||
| chr7:80134662-80134879 | Common:2; Rare:84 | ||||
| chr7:80918910-80919347 | Common:3; Rare:141 | ||||
| chr7:82443543-82443887 | Common:2; Rare:107 |