| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:16645649-16646243 | Common:5; Rare:208 | ||||
| chr7:17298479-17298659 | Common:2; Rare:41 | ||||
| chr7:17940412-17940574 | Common:1; Rare:85 | ||||
| chr7:20217365-20217584 | Common:1; Rare:51 | ||||
| chr7:20331719-20331780 | Common:1; Rare:19 | ||||
| chr7:21427836-21428113 | Common:1; Rare:103 | ||||
| chr7:22822766-22822963 | Common:3; Rare:74 | ||||
| chr7:23105697-23105829 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181711-23182083 | Common:2; Rare:128 | ||||
| chr7:23470362-23470560 | Rare:58 | ||||
| chr7:25125245-25125643 | Rare:156; Clinvar:3 | ||||
| chr7:26201111-26201555 | Common:1; Rare:179 | ||||
| chr7:26201577-26201796 | Common:2; Rare:117 | ||||
| chr7:27096011-27096212 | Rare:60 | ||||
| chr7:27740070-27740199 | Common:5; Rare:31 |