| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:2242168-2242268 | Common:2; Rare:60 | ||||
| chr7:2403304-2403622 | Common:1; Rare:124 | ||||
| chr7:4775478-4775652 | Common:6; Rare:74; Clinvar:1 | ||||
| chr7:5513741-5513837 | Common:1; Rare:47 | ||||
| chr7:5592694-5592825 | Common:1; Rare:47 | ||||
| chr7:6009030-6009469 | Common:4; Rare:199; Clinvar:5; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
| chr7:6484043-6484278 | Common:2; Rare:118 | ||||
| chr7:6577382-6577495 | Rare:35 | ||||
| chr7:7182381-7182679 | Common:3; Rare:109 | ||||
| chr7:7566979-7567037 | Rare:19 | ||||
| chr7:8262028-8262307 | Rare:117 | ||||
| chr7:12211160-12211395 | Common:3; Rare:107 | ||||
| chr7:15686549-15686738 | Common:2; Rare:54 | ||||
| chr7:15686775-15686810 | Rare:10 | ||||
| chr7:16645819-16646214 | Common:4; Rare:133 |