| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:112206328-112206751 | Common:2; Rare:143 | ||||
| chr7:112450156-112450465 | Common:6; Rare:88 | ||||
| chr7:112939753-112940107 | Common:4; Rare:110 | ||||
| chr7:116499508-116499823 | Common:3; Rare:110 | ||||
| chr7:116524749-116525165 | Common:3; Rare:124; Clinvar (benign):2 | ||||
| chr7:116525656-116525782 | Rare:31 | ||||
| chr7:118183965-118184199 | Common:2; Rare:89 | ||||
| chr7:120988645-120988950 | Common:1; Rare:62 | ||||
| chr7:121062742-121062870 | Common:3; Rare:21 | ||||
| chr7:121396204-121396488 | Rare:88 | ||||
| chr7:122144229-122144415 | Common:1; Rare:39 | ||||
| chr7:123534573-123534797 | Common:4; Rare:47 | ||||
| chr7:123748915-123749278 | Common:3; Rare:132 | ||||
| chr7:124929800-124929933 | Common:3; Rare:44 | ||||
| chr7:127585584-127585656 | Rare:24 |