| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:23470362-23470580 | Common:1; Rare:65 | ||||
| chr7:23531954-23532083 | Common:1; Rare:51 | ||||
| chr7:24757406-24757636 | Common:1; Rare:68 | ||||
| chr7:25125275-25125643 | Rare:138; Clinvar:2 | ||||
| chr7:26201417-26201810 | Common:2; Rare:187 | ||||
| chr7:26864535-26864840 | Common:3; Rare:94 | ||||
| chr7:27095976-27096190 | Rare:63 | ||||
| chr7:27150948-27151039 | Rare:23 | ||||
| chr7:27152576-27152729 | Rare:28 | ||||
| chr7:27170361-27170535 | Rare:32 | ||||
| chr7:27185198-27185429 | Common:1; Rare:84 | ||||
| chr7:27740055-27740199 | Common:5; Rare:39 | ||||
| chr7:29989732-29989964 | Rare:87 | ||||
| chr7:30478689-30478820 | Common:1; Rare:47 | ||||
| chr7:30594732-30594949 | Common:3; Rare:102; Clinvar:5; Clinvar (benign):6 |