| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:26200573-26200813 | Common:1; Rare:130 | ||||
| chr7:26201558-26201824 | Common:2; Rare:141 | ||||
| chr7:26292907-26293084 | Rare:34 | ||||
| chr7:26864376-26864659 | Common:2; Rare:79 | ||||
| chr7:27095975-27096147 | Rare:49 | ||||
| chr7:27740034-27740228 | Common:5; Rare:61 | ||||
| chr7:28180510-28180535 | Rare:6 | ||||
| chr7:28685885-28686179 | Common:1; Rare:66 | ||||
| chr7:30594713-30595116 | Common:7; Rare:181; Clinvar:10; Clinvar (benign):15 | ||||
| chr7:32495274-32495564 | Rare:71 | ||||
| chr7:35694895-35695263 | Common:3; Rare:105 | ||||
| chr7:35800606-35800790 | Rare:51 | ||||
| chr7:36724164-36724206 | Rare:8 | ||||
| chr7:36724362-36724583 | Common:2; Rare:48 | ||||
| chr7:39623514-39623726 | Rare:75 |