| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:23304540-23304733 | Common:2; Rare:41 | ||||
| chr7:23308486-23308578 | Rare:21 | ||||
| chr7:23308752-23308837 | Common:1; Rare:18 | ||||
| chr7:23406101-23406122 | Common:1; Rare:3 | ||||
| chr7:23471106-23471489 | Common:2; Rare:112 | ||||
| chr7:23490417-23490646 | Common:3; Rare:109 | ||||
| chr7:23522938-23523209 | Rare:54 | ||||
| chr7:23680816-23680889 | Common:2; Rare:19 | ||||
| chr7:23695438-23695649 | Common:4; Rare:38 | ||||
| chr7:24736549-24736573 | Rare:5 | ||||
| chr7:26193034-26193712 | Common:1; Rare:247; Clinvar (benign):2 | ||||
| chr7:26199178-26199386 | Rare:79 | ||||
| chr7:27785298-27785485 | Rare:50 | ||||
| chr7:27797252-27797293 | Rare:11 | ||||
| chr7:29684861-29685161 | Common:4; Rare:102 |