| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:76303645-76303864 | Common:1; Rare:98; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):7 | ||||
| chr7:76393134-76393346 | Common:1; Rare:76 | ||||
| chr7:77122314-77122674 | Common:2; Rare:74 | ||||
| chr7:77536846-77537240 | Common:9; Rare:107 | ||||
| chr7:77537292-77537636 | Rare:106 | ||||
| chr7:77696127-77696484 | Common:1; Rare:134 | ||||
| chr7:77696903-77697229 | Common:2; Rare:119 | ||||
| chr7:77798249-77798998 | Common:2; Rare:168 | ||||
| chr7:79452811-79453139 | Common:2; Rare:79; Clinvar (benign):2 | ||||
| chr7:79453377-79454141 | Common:5; Rare:185 | ||||
| chr7:82443381-82443395 | Rare:7 | ||||
| chr7:84194577-84195222 | Common:9; Rare:115 | ||||
| chr7:85186694-85187244 | Common:6; Rare:108 | ||||
| chr7:87059640-87059853 | Common:1; Rare:73 | ||||
| chr7:87152314-87152912 | Common:3; Rare:178 |