| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:117872167-117872433 | Common:3; Rare:50 | ||||
| chr7:118183964-118184199 | Common:2; Rare:89 | ||||
| chr7:120950500-120950839 | Common:2; Rare:106 | ||||
| chr7:122144178-122144433 | Common:1; Rare:52 | ||||
| chr7:123534543-123534833 | Common:5; Rare:62 | ||||
| chr7:123557773-123557996 | Common:1; Rare:54 | ||||
| chr7:123748764-123748813 | Rare:15 | ||||
| chr7:123748899-123749278 | Common:3; Rare:137 | ||||
| chr7:124929795-124929886 | Common:2; Rare:25 | ||||
| chr7:124929892-124929985 | Common:1; Rare:30 | ||||
| chr7:127585563-127585671 | Common:2; Rare:41 | ||||
| chr7:127588268-127588495 | Rare:96 | ||||
| chr7:127651830-127652206 | Common:3; Rare:107 | ||||
| chr7:128409950-128410067 | Common:1; Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:128455605-128455909 | Common:4; Rare:129 |