| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:5513768-5513862 | Common:1; Rare:41 | ||||
| chr7:6009030-6009323 | Common:3; Rare:122; Clinvar:3; Clinvar (benign):13 | ||||
| chr7:6104627-6105009 | Common:5; Rare:135 | ||||
| chr7:6447940-6448055 | Common:1; Rare:39 | ||||
| chr7:6483985-6484250 | Common:2; Rare:123 | ||||
| chr7:6577400-6577503 | Rare:38 | ||||
| chr7:7182395-7182705 | Common:3; Rare:115 | ||||
| chr7:7566806-7567025 | Common:4; Rare:91 | ||||
| chr7:8262130-8262291 | Rare:72 | ||||
| chr7:15686549-15686738 | Common:2; Rare:54 | ||||
| chr7:16645712-16646217 | Common:4; Rare:180 | ||||
| chr7:17298461-17298664 | Common:2; Rare:47 | ||||
| chr7:17940398-17940584 | Common:1; Rare:92 | ||||
| chr7:20217371-20217585 | Common:1; Rare:50 | ||||
| chr7:20331738-20331842 | Common:1; Rare:37 |