| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:23181912-23182068 | Rare:65 | ||||
| chr7:23470333-23470563 | Rare:72 | ||||
| chr7:23597297-23597412 | Rare:37 | ||||
| chr7:24757395-24757488 | Common:2; Rare:30 | ||||
| chr7:24980114-24980398 | Common:6; Rare:121 | ||||
| chr7:25125212-25125585 | Rare:156; Clinvar:3 | ||||
| chr7:26201384-26201810 | Common:2; Rare:200 | ||||
| chr7:27185185-27185395 | Common:1; Rare:82 | ||||
| chr7:27740083-27740209 | Common:3; Rare:32 | ||||
| chr7:28686079-28686158 | Rare:18 | ||||
| chr7:29563661-29563842 | Common:1; Rare:49 | ||||
| chr7:30504779-30505043 | Common:1; Rare:84 | ||||
| chr7:30594717-30594949 | Common:3; Rare:106; Clinvar:6; Clinvar (benign):6 | ||||
| chr7:32495240-32495548 | Rare:79 | ||||
| chr7:35800901-35801247 | Common:2; Rare:144 |