| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:6009029-6009350 | Common:4; Rare:136; Clinvar:3; Clinvar (benign):15 | ||||
| chr7:6104627-6105002 | Common:5; Rare:134 | ||||
| chr7:6447961-6448071 | Common:1; Rare:34 | ||||
| chr7:6706929-6707099 | Rare:67 | ||||
| chr7:7182345-7182729 | Common:4; Rare:139 | ||||
| chr7:7566979-7567037 | Rare:19 | ||||
| chr7:10973772-10973915 | Rare:64 | ||||
| chr7:12211160-12211395 | Common:3; Rare:107 | ||||
| chr7:12687422-12687643 | Common:5; Rare:70 | ||||
| chr7:16421218-16421419 | Common:1; Rare:51; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr7:16645832-16646196 | Common:3; Rare:121 | ||||
| chr7:17298413-17298731 | Common:4; Rare:89 | ||||
| chr7:17940412-17940574 | Common:1; Rare:85 | ||||
| chr7:20331719-20331861 | Common:1; Rare:48 | ||||
| chr7:21427797-21428140 | Common:3; Rare:127 |