| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:66682028-66682182 | Common:5; Rare:74 | ||||
| chr7:66996569-66996911 | Common:2; Rare:78 | ||||
| chr7:73683428-73683659 | Common:3; Rare:104 | ||||
| chr7:73738752-73738998 | Common:1; Rare:80 | ||||
| chr7:74174127-74174408 | Common:1; Rare:149 | ||||
| chr7:74254315-74254541 | Rare:108 | ||||
| chr7:75914925-75915162 | Common:3; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:75994497-75994772 | Common:4; Rare:136 | ||||
| chr7:76047945-76048201 | Common:2; Rare:89 | ||||
| chr7:76302873-76303075 | Rare:84; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr7:76303467-76303831 | Common:2; Rare:157; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:77696133-77696465 | Common:1; Rare:122 | ||||
| chr7:77798320-77798971 | Common:1; Rare:152 | ||||
| chr7:79453589-79453634 | Rare:16 | ||||
| chr7:87152309-87152468 | Common:1; Rare:50 |