| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:519105-519312 | Rare:53 | ||||
| chr7:727249-727281 | Rare:10; Clinvar:1 | ||||
| chr7:1028297-1028522 | Common:1; Rare:83 | ||||
| chr7:1055123-1055372 | Common:1; Rare:83 | ||||
| chr7:1138238-1138511 | Common:2; Rare:75 | ||||
| chr7:1570018-1570146 | Common:1; Rare:43 | ||||
| chr7:2242178-2242256 | Common:2; Rare:46 | ||||
| chr7:4775391-4775693 | Common:7; Rare:143; Clinvar:1 | ||||
| chr7:5425425-5425770 | Rare:99 | ||||
| chr7:5513768-5513855 | Common:1; Rare:39 | ||||
| chr7:5529805-5530047 | Common:1; Rare:103 | ||||
| chr7:6009026-6009355 | Common:4; Rare:139; Clinvar:4; Clinvar (benign):15 | ||||
| chr7:6399912-6400183 | Rare:57 | ||||
| chr7:7566703-7567033 | Common:5; Rare:131 | ||||
| chr7:8262143-8262294 | Rare:65 |