| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:16645629-16646208 | Common:3; Rare:199 | ||||
| chr7:20331728-20331777 | Common:1; Rare:15 | ||||
| chr7:22822766-22822954 | Common:3; Rare:69 | ||||
| chr7:23105667-23105886 | Common:4; Rare:113; Clinvar:3; Clinvar (benign):3 | ||||
| chr7:23181853-23182107 | Common:2; Rare:103 | ||||
| chr7:23470362-23470557 | Rare:58 | ||||
| chr7:23531954-23532116 | Common:1; Rare:63 | ||||
| chr7:23597310-23597392 | Rare:30 | ||||
| chr7:24757403-24757572 | Common:2; Rare:53 | ||||
| chr7:25125242-25125633 | Rare:155; Clinvar:3 | ||||
| chr7:26200593-26200941 | Common:1; Rare:169 | ||||
| chr7:26200975-26201805 | Common:3; Rare:368 | ||||
| chr7:26864546-26864840 | Common:3; Rare:89 | ||||
| chr7:27096023-27096212 | Rare:53 | ||||
| chr7:27172795-27173010 | Rare:53 |