| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:1570018-1570125 | Common:1; Rare:34 | ||||
| chr7:2242177-2242245 | Common:2; Rare:41 | ||||
| chr7:4775497-4775652 | Common:6; Rare:62; Clinvar:1 | ||||
| chr7:5513752-5513855 | Common:1; Rare:49 | ||||
| chr7:6009030-6009350 | Common:4; Rare:135; Clinvar:3; Clinvar (benign):14 | ||||
| chr7:7566740-7566993 | Common:5; Rare:109 | ||||
| chr7:8262130-8262291 | Rare:72 | ||||
| chr7:8262524-8262619 | Common:1; Rare:30 | ||||
| chr7:12211167-12211395 | Common:3; Rare:104 | ||||
| chr7:16645721-16645799 | Rare:38 | ||||
| chr7:16645819-16646220 | Common:4; Rare:136 | ||||
| chr7:16881959-16882122 | Rare:41 | ||||
| chr7:17940401-17940571 | Common:1; Rare:85 | ||||
| chr7:20217375-20217577 | Common:1; Rare:46 | ||||
| chr7:23105673-23105831 | Common:3; Rare:83; Clinvar:2; Clinvar (benign):3 |