| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:27740061-27740199 | Common:5; Rare:36 | ||||
| chr7:29989726-29989898 | Rare:68 | ||||
| chr7:30504751-30505081 | Common:2; Rare:109 | ||||
| chr7:30594717-30594950 | Common:3; Rare:108; Clinvar:6; Clinvar (benign):6 | ||||
| chr7:32070785-32071126 | Common:3; Rare:84 | ||||
| chr7:32490354-32490479 | Rare:38 | ||||
| chr7:32495238-32495554 | Rare:82 | ||||
| chr7:33062707-33062909 | Common:3; Rare:87 | ||||
| chr7:35800722-35801269 | Common:2; Rare:209 | ||||
| chr7:37342827-37342859 | Rare:6 | ||||
| chr7:39566353-39566458 | Common:1; Rare:50 | ||||
| chr7:39623503-39623807 | Rare:95 | ||||
| chr7:40134555-40135016 | Rare:145; Clinvar:1 | ||||
| chr7:42932130-42932457 | Rare:132 | ||||
| chr7:43249002-43249153 | Common:2; Rare:39 |