| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:130051318-130051447 | Rare:56 | ||||
| chr7:130205377-130205520 | Rare:66 | ||||
| chr7:130441001-130441338 | Common:3; Rare:141; Clinvar:2; Clinvar (benign):2 | ||||
| chr7:131109857-131110101 | Common:1; Rare:43 | ||||
| chr7:131327697-131327909 | Rare:66 | ||||
| chr7:134316776-134317175 | Common:2; Rare:108 | ||||
| chr7:134527310-134527604 | Common:1; Rare:44 | ||||
| chr7:134646535-134646922 | Common:10; Rare:128 | ||||
| chr7:134660565-134660760 | Common:1; Rare:30 | ||||
| chr7:135148016-135148229 | Rare:48 | ||||
| chr7:135170452-135170857 | Common:3; Rare:146 | ||||
| chr7:135211426-135211750 | Common:2; Rare:153 | ||||
| chr7:135557647-135557947 | Common:3; Rare:84 | ||||
| chr7:135662361-135662556 | Common:3; Rare:91 | ||||
| chr7:138002021-138002336 | Common:2; Rare:79 |