| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:16645625-16646220 | Common:4; Rare:203 | ||||
| chr7:16662054-16662230 | Common:1; Rare:37 | ||||
| chr7:17298444-17298717 | Common:3; Rare:73 | ||||
| chr7:17940387-17940584 | Common:1; Rare:98 | ||||
| chr7:18086692-18087004 | Common:4; Rare:126 | ||||
| chr7:18495617-18495833 | Rare:50 | ||||
| chr7:20330755-20331061 | Common:2; Rare:83 | ||||
| chr7:20331733-20331856 | Common:1; Rare:43 | ||||
| chr7:21427845-21428244 | Common:4; Rare:155 | ||||
| chr7:22220173-22220359 | Common:2; Rare:31 | ||||
| chr7:22822704-22822963 | Common:3; Rare:99 | ||||
| chr7:23105661-23105972 | Common:4; Rare:141; Clinvar:3; Clinvar (benign):3 | ||||
| chr7:23106394-23106751 | Common:2; Rare:69 | ||||
| chr7:23181746-23181812 | Rare:12 | ||||
| chr7:23181818-23182169 | Common:2; Rare:145 |