| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:74890532-74890820 | Common:2; Rare:92 | ||||
| chr7:75358982-75359263 | Common:1; Rare:9 | ||||
| chr7:75410235-75410362 | Rare:12 | ||||
| chr7:76304182-76304510 | Common:5; Rare:104; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:77245476-77245569 | Rare:13 | ||||
| chr7:80637632-80637741 | Common:2; Rare:16 | ||||
| chr7:80644240-80644559 | Common:1; Rare:47 | ||||
| chr7:82410526-82410820 | Common:3; Rare:68 | ||||
| chr7:90597395-90597447 | Rare:8 | ||||
| chr7:91263316-91263571 | Common:1; Rare:46 | ||||
| chr7:91266471-91266739 | Common:1; Rare:83 | ||||
| chr7:91267623-91267777 | Rare:28 | ||||
| chr7:97972254-97972392 | Common:1; Rare:35 | ||||
| chr7:100335862-100336146 | Common:1; Rare:94 | ||||
| chr7:101953590-101953751 | Rare:34 |