| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:18509104-18509372 | Rare:52 | ||||
| chr7:19708971-19709152 | Common:3; Rare:76 | ||||
| chr7:20217375-20217586 | Common:1; Rare:48 | ||||
| chr7:20331739-20331834 | Common:1; Rare:33 | ||||
| chr7:21427824-21428115 | Common:3; Rare:106 | ||||
| chr7:22726986-22727235 | Common:2; Rare:34 | ||||
| chr7:22727275-22727541 | Common:2; Rare:92 | ||||
| chr7:22822766-22822969 | Common:3; Rare:77 | ||||
| chr7:23105675-23105825 | Common:2; Rare:79; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181802-23182077 | Common:2; Rare:106 | ||||
| chr7:23470362-23470543 | Rare:55 | ||||
| chr7:23531958-23532082 | Common:1; Rare:48 | ||||
| chr7:24757383-24757552 | Common:3; Rare:56 | ||||
| chr7:25125241-25125589 | Rare:138; Clinvar:3 | ||||
| chr7:26200661-26201034 | Common:2; Rare:187 |