| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:122144208-122144433 | Common:1; Rare:48 | ||||
| chr7:123748738-123749238 | Common:3; Rare:177 | ||||
| chr7:124929776-124929904 | Common:2; Rare:40 | ||||
| chr7:127585150-127585418 | Common:1; Rare:62 | ||||
| chr7:127589004-127589136 | Rare:42 | ||||
| chr7:128455750-128455873 | Common:2; Rare:68 | ||||
| chr7:128830171-128830440 | Common:4; Rare:71 | ||||
| chr7:129611625-129611805 | Common:1; Rare:58 | ||||
| chr7:131109857-131110129 | Common:1; Rare:50 | ||||
| chr7:131327657-131327894 | Rare:71 | ||||
| chr7:134646584-134646856 | Common:5; Rare:77 | ||||
| chr7:135148022-135148113 | Rare:24 | ||||
| chr7:135170623-135170781 | Common:1; Rare:62 | ||||
| chr7:136869077-136869096 | Rare:5 | ||||
| chr7:136869132-136869264 | Common:1; Rare:26; Clinvar (benign):2 |