| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:91940735-91940979 | Common:4; Rare:75; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:92134364-92134598 | Rare:74 | ||||
| chr7:92134709-92134908 | Common:3; Rare:57 | ||||
| chr7:92245648-92246274 | Common:6; Rare:153; Clinvar:4; Clinvar (benign):5 | ||||
| chr7:92528361-92528829 | Common:4; Rare:146; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92590030-92590159 | Common:1; Rare:48 | ||||
| chr7:92833902-92834007 | Rare:28 | ||||
| chr7:92836364-92836498 | Rare:25 | ||||
| chr7:93117948-93118106 | Rare:27 | ||||
| chr7:93148359-93148679 | Common:1; Rare:47 | ||||
| chr7:93232200-93232431 | Common:3; Rare:49 | ||||
| chr7:93590987-93591734 | Common:7; Rare:253 | ||||
| chr7:93591765-93591822 | Rare:15 | ||||
| chr7:93890589-93890988 | Common:4; Rare:112 | ||||
| chr7:93921631-93922182 | Common:7; Rare:128 |