| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:74174104-74174412 | Common:1; Rare:157 | ||||
| chr7:74254373-74254526 | Rare:69 | ||||
| chr7:74657459-74657731 | Common:2; Rare:80 | ||||
| chr7:75914911-75915164 | Common:3; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:76047943-76048211 | Common:2; Rare:92 | ||||
| chr7:76302884-76303024 | Rare:65; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr7:76303026-76303058 | Rare:10; Clinvar (benign):1 | ||||
| chr7:76627248-76627352 | Common:3; Rare:31 | ||||
| chr7:77122287-77122642 | Common:2; Rare:73 | ||||
| chr7:77199795-77199849 | Rare:18 | ||||
| chr7:77696133-77696480 | Common:1; Rare:129 | ||||
| chr7:77798455-77798971 | Common:1; Rare:129 | ||||
| chr7:79453612-79454106 | Common:3; Rare:121 | ||||
| chr7:87152280-87152655 | Common:2; Rare:118 | ||||
| chr7:87345452-87345701 | Common:4; Rare:84 |