| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:27740022-27740192 | Common:5; Rare:54 | ||||
| chr7:28409149-28409387 | Common:1; Rare:62 | ||||
| chr7:29989727-29989890 | Rare:64 | ||||
| chr7:30504762-30505090 | Common:2; Rare:108 | ||||
| chr7:30594732-30594959 | Common:3; Rare:108; Clinvar:5; Clinvar (benign):6 | ||||
| chr7:32490354-32490479 | Rare:38 | ||||
| chr7:32495238-32495600 | Common:1; Rare:94 | ||||
| chr7:33062707-33062910 | Common:3; Rare:87 | ||||
| chr7:33129220-33129587 | Common:5; Rare:105 | ||||
| chr7:35800586-35800703 | Rare:29 | ||||
| chr7:35800928-35801252 | Common:2; Rare:135 | ||||
| chr7:38178025-38178396 | Common:3; Rare:107 | ||||
| chr7:39566326-39566449 | Common:1; Rare:58 | ||||
| chr7:39623460-39623819 | Rare:115 | ||||
| chr7:40134581-40135032 | Rare:141; Clinvar:1 |