| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:66682007-66682229 | Common:6; Rare:102 | ||||
| chr7:66995292-66995705 | Rare:142; Clinvar (benign):1; Clinvar (pathogenic):5 | ||||
| chr7:66996557-66996966 | Common:2; Rare:108 | ||||
| chr7:73557104-73557372 | Common:1; Rare:97 | ||||
| chr7:73683390-73683661 | Common:3; Rare:125 | ||||
| chr7:73738768-73739099 | Common:2; Rare:108 | ||||
| chr7:74027977-74028202 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:74174029-74174441 | Common:1; Rare:176 | ||||
| chr7:74209721-74210021 | Common:1; Rare:73 | ||||
| chr7:74254328-74254535 | Rare:95 | ||||
| chr7:74453707-74454024 | Common:1; Rare:83 | ||||
| chr7:74657506-74657738 | Common:2; Rare:69 | ||||
| chr7:74657837-74658067 | Common:1; Rare:50 | ||||
| chr7:75878853-75879088 | Common:12; Rare:87 | ||||
| chr7:75914944-75915189 | Common:2; Rare:89; Clinvar:3; Clinvar (benign):1 |