| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:170554221-170554420 | Common:1; Rare:64 | ||||
| chr7:727241-727281 | Rare:14; Clinvar:1 | ||||
| chr7:1570012-1570087 | Common:1; Rare:24 | ||||
| chr7:2242171-2242270 | Common:2; Rare:58 | ||||
| chr7:4775375-4775645 | Common:7; Rare:118 | ||||
| chr7:6009029-6009323 | Common:3; Rare:123; Clinvar:3; Clinvar (benign):14 | ||||
| chr7:6447940-6448047 | Rare:37 | ||||
| chr7:6577382-6577489 | Rare:31 | ||||
| chr7:12403856-12403987 | Common:1; Rare:30 | ||||
| chr7:12686615-12686906 | Common:3; Rare:87 | ||||
| chr7:13989122-13989336 | Common:2; Rare:48 | ||||
| chr7:16645707-16646109 | Common:1; Rare:141 | ||||
| chr7:17940398-17940603 | Common:2; Rare:98 | ||||
| chr7:22822748-22822969 | Common:3; Rare:85 | ||||
| chr7:23105673-23105897 | Common:3; Rare:113; Clinvar:3; Clinvar (benign):3 |