| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:73521955-73522031 | Rare:26 | ||||
| chr7:73683405-73683668 | Common:3; Rare:120 | ||||
| chr7:74174093-74174441 | Common:1; Rare:161 | ||||
| chr7:74254373-74254523 | Rare:67 | ||||
| chr7:75914917-75915189 | Common:3; Rare:98; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:75994498-75994772 | Common:4; Rare:135 | ||||
| chr7:76047950-76048220 | Common:2; Rare:94 | ||||
| chr7:76302815-76303075 | Rare:114; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr7:76303684-76303865 | Common:1; Rare:82; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):7 | ||||
| chr7:76358720-76358895 | Rare:54 | ||||
| chr7:77696133-77696527 | Common:1; Rare:162 | ||||
| chr7:77798353-77798986 | Common:1; Rare:150 | ||||
| chr7:79453552-79454109 | Common:3; Rare:137 | ||||
| chr7:80602158-80602342 | Common:1; Rare:36; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:87152309-87152474 | Common:1; Rare:54 |