| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:116499539-116499779 | Common:3; Rare:85 | ||||
| chr7:116524748-116525049 | Rare:80 | ||||
| chr7:116672231-116672519 | Common:1; Rare:67; Clinvar:2 | ||||
| chr7:118183965-118184199 | Common:2; Rare:89 | ||||
| chr7:118214566-118214667 | Common:1; Rare:33 | ||||
| chr7:120950509-120950819 | Common:2; Rare:98 | ||||
| chr7:121396224-121396616 | Common:1; Rare:135 | ||||
| chr7:123557773-123557969 | Common:1; Rare:51 | ||||
| chr7:123748925-123749223 | Common:3; Rare:106 | ||||
| chr7:124929806-124929921 | Common:3; Rare:40 | ||||
| chr7:127585584-127585689 | Rare:33 | ||||
| chr7:128476656-128476805 | Rare:56 | ||||
| chr7:128739152-128739425 | Common:2; Rare:73 | ||||
| chr7:128830581-128830709 | Rare:60; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:129054884-129055231 | Common:2; Rare:66 |