| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:7566776-7567025 | Common:4; Rare:105 | ||||
| chr7:12686733-12686906 | Common:2; Rare:53 | ||||
| chr7:16645832-16646140 | Common:2; Rare:100 | ||||
| chr7:17298526-17298712 | Common:1; Rare:49 | ||||
| chr7:20331719-20331834 | Common:1; Rare:38 | ||||
| chr7:23105687-23105865 | Common:2; Rare:99; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181860-23182088 | Common:2; Rare:92 | ||||
| chr7:23531966-23532083 | Rare:47 | ||||
| chr7:24980108-24980389 | Common:6; Rare:117 | ||||
| chr7:26200697-26201003 | Common:1; Rare:156 | ||||
| chr7:26201383-26201555 | Rare:64 | ||||
| chr7:27095956-27096256 | Rare:77 | ||||
| chr7:27179824-27179967 | Rare:56 | ||||
| chr7:27740085-27740209 | Common:3; Rare:32 | ||||
| chr7:29563687-29563833 | Rare:39 |