| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:66682028-66682167 | Common:5; Rare:66 | ||||
| chr7:66996576-66996888 | Common:2; Rare:64 | ||||
| chr7:73683419-73683668 | Common:3; Rare:112 | ||||
| chr7:73738779-73739109 | Common:2; Rare:107 | ||||
| chr7:74174124-74174419 | Common:1; Rare:153 | ||||
| chr7:74254335-74254528 | Rare:90 | ||||
| chr7:75611763-75611977 | Common:1; Rare:41 | ||||
| chr7:76047950-76048220 | Common:2; Rare:94 | ||||
| chr7:76302820-76303073 | Rare:111; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr7:77696236-77696465 | Rare:91 | ||||
| chr7:77798353-77798773 | Common:1; Rare:83 | ||||
| chr7:79453586-79454115 | Common:3; Rare:132 | ||||
| chr7:87152329-87152470 | Common:1; Rare:48 | ||||
| chr7:87345416-87345706 | Common:4; Rare:90 | ||||
| chr7:87876224-87876658 | Common:3; Rare:186 |