| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:26201565-26201853 | Common:2; Rare:145 | ||||
| chr7:26864447-26864659 | Common:1; Rare:58 | ||||
| chr7:27096001-27096125 | Rare:35 | ||||
| chr7:27143588-27143600 | Rare:1 | ||||
| chr7:27143651-27143702 | Rare:10 | ||||
| chr7:27156237-27156538 | Common:3; Rare:123 | ||||
| chr7:27165491-27165587 | Common:2; Rare:36 | ||||
| chr7:27662772-27662990 | Common:3; Rare:89 | ||||
| chr7:27740073-27740212 | Common:4; Rare:36 | ||||
| chr7:28685985-28686152 | Rare:42 | ||||
| chr7:29563676-29563784 | Rare:30 | ||||
| chr7:29989713-29989826 | Rare:46 | ||||
| chr7:30504762-30504976 | Common:1; Rare:78 | ||||
| chr7:30594706-30595113 | Common:7; Rare:182; Clinvar:10; Clinvar (benign):15 | ||||
| chr7:32495256-32495548 | Rare:74 |