| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:35694892-35695268 | Common:4; Rare:107 | ||||
| chr7:35800939-35801266 | Common:2; Rare:139 | ||||
| chr7:36389752-36389960 | Common:1; Rare:68 | ||||
| chr7:38178074-38178405 | Common:3; Rare:99 | ||||
| chr7:39566288-39566474 | Common:1; Rare:90 | ||||
| chr7:39623501-39623820 | Rare:99 | ||||
| chr7:39949348-39949722 | Common:2; Rare:135 | ||||
| chr7:39949905-39950032 | Rare:34 | ||||
| chr7:39951592-39951829 | Rare:97; Clinvar (benign):1 | ||||
| chr7:40134417-40134517 | Rare:49 | ||||
| chr7:40134558-40135075 | Common:1; Rare:163; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:41692258-41692626 | Rare:69 | ||||
| chr7:41700280-41700833 | Common:1; Rare:105 | ||||
| chr7:41702923-41703279 | Common:2; Rare:56 | ||||
| chr7:42932148-42932495 | Rare:134 |