| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:7968571-7968796 | Common:1; Rare:78 | ||||
| chr7:8262024-8262274 | Rare:100 | ||||
| chr7:10939827-10939902 | Rare:19 | ||||
| chr7:10940017-10940220 | Common:1; Rare:96; Clinvar (benign):3 | ||||
| chr7:10940438-10940550 | Common:1; Rare:43 | ||||
| chr7:10973609-10973919 | Common:1; Rare:135 | ||||
| chr7:12211166-12211470 | Common:3; Rare:119 | ||||
| chr7:12403546-12404006 | Common:3; Rare:150 | ||||
| chr7:12686689-12686906 | Common:2; Rare:69 | ||||
| chr7:13988152-13988217 | Common:1; Rare:20 | ||||
| chr7:13988495-13989006 | Common:7; Rare:119 | ||||
| chr7:16465736-16465947 | Rare:35 | ||||
| chr7:16645425-16645469 | Common:3; Rare:25 | ||||
| chr7:16645521-16646272 | Common:6; Rare:267 | ||||
| chr7:16662054-16662221 | Common:1; Rare:35 |