| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:6104627-6105002 | Common:5; Rare:134 | ||||
| chr7:6447919-6448066 | Common:1; Rare:51 | ||||
| chr7:7566786-7567051 | Common:4; Rare:107 | ||||
| chr7:8262102-8262310 | Rare:93 | ||||
| chr7:8262443-8262589 | Common:2; Rare:49 | ||||
| chr7:12211180-12211425 | Common:3; Rare:101 | ||||
| chr7:12687431-12687644 | Common:5; Rare:68 | ||||
| chr7:15686543-15686738 | Common:2; Rare:55 | ||||
| chr7:16645629-16646140 | Common:2; Rare:169 | ||||
| chr7:16662075-16662226 | Common:1; Rare:35 | ||||
| chr7:17298444-17298712 | Common:3; Rare:71 | ||||
| chr7:17940412-17940584 | Common:1; Rare:88 | ||||
| chr7:21542951-21543121 | Common:1; Rare:59 | ||||
| chr7:22822676-22822964 | Common:3; Rare:109 | ||||
| chr7:23105675-23105871 | Common:2; Rare:105; Clinvar:2; Clinvar (benign):3 |