| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:19708784-19708906 | Rare:41 | ||||
| chr7:20331703-20331824 | Common:2; Rare:38 | ||||
| chr7:22726231-22726256 | Rare:3 | ||||
| chr7:22726986-22727217 | Common:2; Rare:26 | ||||
| chr7:22727620-22727658 | Rare:10 | ||||
| chr7:22822707-22822904 | Common:2; Rare:83 | ||||
| chr7:23105661-23106049 | Common:4; Rare:164; Clinvar:5; Clinvar (benign):3 | ||||
| chr7:23181806-23182207 | Common:3; Rare:163 | ||||
| chr7:23299302-23299394 | Common:1; Rare:69 | ||||
| chr7:23467901-23468094 | Common:2; Rare:47 | ||||
| chr7:23470163-23470570 | Common:1; Rare:116 | ||||
| chr7:23470812-23470883 | Rare:12 | ||||
| chr7:23531788-23532083 | Common:2; Rare:115 | ||||
| chr7:23597319-23597510 | Common:1; Rare:69 | ||||
| chr7:24757374-24757586 | Common:3; Rare:64 |