| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:76047985-76048163 | Common:1; Rare:54 | ||||
| chr7:76302440-76302576 | Rare:35 | ||||
| chr7:76302581-76303286 | Common:5; Rare:294; Clinvar:19; Clinvar (benign):13; Clinvar (pathogenic):5 | ||||
| chr7:76303823-76304129 | Common:2; Rare:150; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):9 | ||||
| chr7:77199803-77199824 | Rare:9 | ||||
| chr7:77199826-77200005 | Common:2; Rare:29 | ||||
| chr7:77696198-77696500 | Common:1; Rare:129 | ||||
| chr7:77798418-77798916 | Common:1; Rare:125 | ||||
| chr7:79453603-79454123 | Common:3; Rare:133 | ||||
| chr7:80918955-80919347 | Common:3; Rare:132 | ||||
| chr7:87152149-87152789 | Common:3; Rare:185 | ||||
| chr7:87220526-87220682 | Common:1; Rare:45 | ||||
| chr7:87345443-87345736 | Common:5; Rare:91 | ||||
| chr7:87876276-87876646 | Common:2; Rare:166 | ||||
| chr7:90211625-90211947 | Common:4; Rare:99 |