| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:73842508-73842716 | Common:5; Rare:31 | ||||
| chr7:74174104-74174441 | Common:1; Rare:160 | ||||
| chr7:74254304-74254535 | Rare:107 | ||||
| chr7:74657462-74657730 | Common:2; Rare:79 | ||||
| chr7:75914902-75915213 | Common:4; Rare:113; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:75994493-75994786 | Common:4; Rare:144 | ||||
| chr7:76047939-76048198 | Common:2; Rare:90 | ||||
| chr7:76302877-76303003 | Rare:60; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr7:76303465-76303817 | Common:2; Rare:149; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr7:76627248-76627361 | Common:5; Rare:31 | ||||
| chr7:77122287-77122568 | Common:1; Rare:54 | ||||
| chr7:77696127-77696475 | Common:1; Rare:128 | ||||
| chr7:77696627-77696978 | Rare:153 | ||||
| chr7:77798353-77798959 | Common:1; Rare:145 | ||||
| chr7:79453549-79454121 | Common:3; Rare:141 |