| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:66921140-66921459 | Common:1; Rare:95 | ||||
| chr7:73308788-73308897 | Rare:39 | ||||
| chr7:73683394-73683631 | Common:3; Rare:101 | ||||
| chr7:74289232-74289434 | Common:3; Rare:71 | ||||
| chr7:75994502-75994773 | Common:4; Rare:135 | ||||
| chr7:76047768-76048197 | Common:3; Rare:127 | ||||
| chr7:76303657-76303856 | Common:1; Rare:90; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):7 | ||||
| chr7:77696253-77696468 | Rare:88 | ||||
| chr7:77798304-77798926 | Common:1; Rare:148 | ||||
| chr7:87345061-87345355 | Common:1; Rare:63 | ||||
| chr7:87345452-87345753 | Common:6; Rare:96 | ||||
| chr7:92134721-92135038 | Common:3; Rare:78 | ||||
| chr7:92528444-92528819 | Common:3; Rare:118; Clinvar:3; Clinvar (benign):2 | ||||
| chr7:93232170-93232381 | Common:2; Rare:45 | ||||
| chr7:94394532-94395095 | Common:1; Rare:106; Clinvar:2; Clinvar (benign):3 |