| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:75878847-75879083 | Common:12; Rare:86 | ||||
| chr7:75914903-75915173 | Common:3; Rare:91; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:75994493-75994772 | Common:4; Rare:137 | ||||
| chr7:76047811-76048204 | Common:3; Rare:122 | ||||
| chr7:76302844-76303075 | Rare:98; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr7:76303487-76303851 | Common:2; Rare:158; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):6 | ||||
| chr7:77696226-77696470 | Rare:99 | ||||
| chr7:77696818-77696891 | Rare:27 | ||||
| chr7:77798344-77798932 | Common:1; Rare:143 | ||||
| chr7:79452641-79452882 | Rare:39 | ||||
| chr7:79452997-79453191 | Common:1; Rare:49; Clinvar (benign):2 | ||||
| chr7:79453538-79453650 | Rare:29 | ||||
| chr7:79453652-79453781 | Common:1; Rare:30 | ||||
| chr7:79453789-79454145 | Common:2; Rare:84 | ||||
| chr7:80134672-80134888 | Common:2; Rare:88 |