| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:79453652-79454085 | Common:3; Rare:106 | ||||
| chr7:80918986-80919277 | Common:3; Rare:92 | ||||
| chr7:87152127-87152453 | Common:2; Rare:89 | ||||
| chr7:87345443-87345701 | Common:4; Rare:85 | ||||
| chr7:87876291-87876574 | Common:2; Rare:126 | ||||
| chr7:90346501-90346752 | Common:4; Rare:103 | ||||
| chr7:91880657-91880791 | Common:1; Rare:39 | ||||
| chr7:91940849-91941011 | Common:3; Rare:57; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:92134456-92134772 | Common:3; Rare:86 | ||||
| chr7:92245895-92245956 | Rare:20; Clinvar:3 | ||||
| chr7:92528397-92528816 | Common:3; Rare:132; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:93890743-93890882 | Common:2; Rare:35 | ||||
| chr7:94394540-94395096 | Common:1; Rare:104; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:94424071-94424460 | Rare:92; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr7:94425725-94426050 | Rare:96; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):1 |