| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:727220-727326 | Rare:36; Clinvar:2 | ||||
| chr7:975519-975654 | Common:1; Rare:55 | ||||
| chr7:1570020-1570134 | Common:1; Rare:37 | ||||
| chr7:2242171-2242265 | Common:2; Rare:55 | ||||
| chr7:2354542-2354933 | Common:5; Rare:164 | ||||
| chr7:2403290-2403631 | Common:1; Rare:134 | ||||
| chr7:2688026-2688280 | Rare:75 | ||||
| chr7:4775524-4775697 | Common:4; Rare:85; Clinvar:1 | ||||
| chr7:5423563-5423606 | Rare:9 | ||||
| chr7:5423691-5424049 | Common:3; Rare:90 | ||||
| chr7:5513718-5513894 | Common:1; Rare:77 | ||||
| chr7:5527662-5528129 | Common:3; Rare:164; Clinvar:1; Clinvar (benign):11; Clinvar (pathogenic):2 | ||||
| chr7:5592674-5592841 | Common:1; Rare:60 | ||||
| chr7:6009023-6009355 | Common:4; Rare:142; Clinvar:6; Clinvar (benign):15 | ||||
| chr7:6447895-6448057 | Common:1; Rare:65 |