| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:170553207-170553377 | Common:3; Rare:72 | ||||
| chr6:170554211-170554416 | Common:1; Rare:65 | ||||
| chr7:727250-727299 | Rare:14; Clinvar:1 | ||||
| chr7:831803-832036 | Common:3; Rare:52 | ||||
| chr7:975496-975674 | Common:1; Rare:79 | ||||
| chr7:1055316-1055372 | Rare:20 | ||||
| chr7:1537288-1537465 | Rare:59 | ||||
| chr7:1570018-1570142 | Common:1; Rare:41 | ||||
| chr7:2242173-2242255 | Common:2; Rare:49 | ||||
| chr7:2403278-2403637 | Common:1; Rare:141 | ||||
| chr7:4775510-4775701 | Common:4; Rare:90; Clinvar:1 | ||||
| chr7:5513768-5513844 | Common:1; Rare:33 | ||||
| chr7:6009030-6009323 | Common:3; Rare:122; Clinvar:3; Clinvar (benign):13 | ||||
| chr7:6104622-6104987 | Common:5; Rare:133 | ||||
| chr7:6401769-6401969 | Rare:42 |