| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:16645600-16646192 | Common:3; Rare:203 | ||||
| chr7:17940439-17940557 | Common:1; Rare:62 | ||||
| chr7:22822707-22822967 | Common:3; Rare:99 | ||||
| chr7:23105655-23105855 | Common:4; Rare:109; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181829-23181867 | Common:1; Rare:11 | ||||
| chr7:23181891-23182190 | Rare:127 | ||||
| chr7:23299193-23299391 | Common:2; Rare:104 | ||||
| chr7:23307809-23307949 | Rare:55 | ||||
| chr7:23467901-23468071 | Common:1; Rare:41 | ||||
| chr7:23470270-23470596 | Common:1; Rare:98 | ||||
| chr7:23531786-23532083 | Common:2; Rare:116 | ||||
| chr7:24757376-24757549 | Common:3; Rare:55 | ||||
| chr7:24980152-24980449 | Common:8; Rare:120 | ||||
| chr7:25125217-25125599 | Rare:159; Clinvar:3 | ||||
| chr7:26196389-26196690 | Common:2; Rare:117; Clinvar (benign):3 |