| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:100101299-100101717 | Common:1; Rare:167; Clinvar (benign):1 | ||||
| chr7:100119257-100119742 | Common:1; Rare:149; Clinvar:1 | ||||
| chr7:100127133-100127266 | Common:1; Rare:35 | ||||
| chr7:100148679-100149046 | Common:1; Rare:159 | ||||
| chr7:100171395-100171784 | Common:1; Rare:128 | ||||
| chr7:100177335-100178005 | Common:2; Rare:150 | ||||
| chr7:100197585-100197833 | Common:1; Rare:51 | ||||
| chr7:100197957-100198159 | Rare:48 | ||||
| chr7:100204727-100205303 | Common:1; Rare:157 | ||||
| chr7:100307540-100307752 | Common:1; Rare:50 | ||||
| chr7:100353216-100353450 | Common:2; Rare:63 | ||||
| chr7:100358474-100358764 | Common:1; Rare:86 | ||||
| chr7:100367127-100367398 | Common:1; Rare:68 | ||||
| chr7:100373232-100373495 | Rare:47 | ||||
| chr7:100428173-100428350 | Common:1; Rare:48 |