| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:30284558-30284792 | Common:4; Rare:114 | ||||
| chr7:30478665-30478938 | Common:5; Rare:96; Clinvar:1 | ||||
| chr7:30504717-30505099 | Common:4; Rare:129 | ||||
| chr7:30594709-30595004 | Common:5; Rare:137; Clinvar:6; Clinvar (benign):10 | ||||
| chr7:30682480-30682600 | Rare:38 | ||||
| chr7:30771299-30771494 | Common:1; Rare:67 | ||||
| chr7:32490342-32490457 | Rare:44 | ||||
| chr7:32495238-32495617 | Common:1; Rare:96 | ||||
| chr7:32957350-32957437 | Common:1; Rare:28 | ||||
| chr7:32988321-32988595 | Common:2; Rare:82 | ||||
| chr7:33040896-33041051 | Common:1; Rare:29 | ||||
| chr7:33062696-33062876 | Common:1; Rare:83 | ||||
| chr7:33109269-33109513 | Rare:81; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:33129227-33129593 | Common:5; Rare:102 | ||||
| chr7:35694846-35695254 | Common:4; Rare:113 |