| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:2242166-2242256 | Common:2; Rare:56 | ||||
| chr7:2354056-2354137 | Rare:35 | ||||
| chr7:2403278-2403637 | Common:1; Rare:141 | ||||
| chr7:2555477-2555838 | Common:5; Rare:99 | ||||
| chr7:2558978-2559137 | Common:2; Rare:72 | ||||
| chr7:4775510-4775720 | Common:4; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:4882207-4882349 | Common:1; Rare:30 | ||||
| chr7:5190122-5190260 | Rare:56 | ||||
| chr7:5423800-5424058 | Common:3; Rare:63 | ||||
| chr7:5513746-5513844 | Common:1; Rare:46 | ||||
| chr7:5592676-5592825 | Common:1; Rare:53 | ||||
| chr7:5898645-5898824 | Common:4; Rare:36 | ||||
| chr7:6009015-6009372 | Common:4; Rare:152; Clinvar:10; Clinvar (benign):15; Clinvar (pathogenic):2 | ||||
| chr7:6059033-6059308 | Common:5; Rare:105 | ||||
| chr7:6104620-6105025 | Common:5; Rare:141 |