| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:143384929-143385183 | Common:2; Rare:49 | ||||
| chr7:143385663-143386038 | Common:1; Rare:69 | ||||
| chr7:143386040-143386355 | Common:2; Rare:64 | ||||
| chr7:143386509-143386814 | Common:4; Rare:58 | ||||
| chr7:143386969-143387113 | Rare:16 | ||||
| chr7:143389821-143390188 | Common:1; Rare:83 | ||||
| chr7:143410771-143410873 | Common:1; Rare:21 | ||||
| chr7:143413983-143414229 | Common:4; Rare:65 | ||||
| chr7:143429951-143430012 | Common:3; Rare:6 | ||||
| chr7:143472490-143472699 | Common:2; Rare:40 | ||||
| chr7:143495064-143495348 | Common:3; Rare:52 | ||||
| chr7:143519593-143519853 | Common:2; Rare:31 | ||||
| chr7:143836639-143836733 | Common:1; Rare:7 | ||||
| chr7:148795833-148795890 | Rare:6 | ||||
| chr7:148807214-148807501 | Common:1; Rare:69; Clinvar (benign):1 |