| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:131327715-131327894 | Rare:63 | ||||
| chr7:134646569-134646873 | Common:6; Rare:91 | ||||
| chr7:135170685-135170774 | Common:1; Rare:36 | ||||
| chr7:135510074-135510321 | Common:2; Rare:54 | ||||
| chr7:135662348-135662511 | Common:4; Rare:67 | ||||
| chr7:139109347-139109604 | Common:1; Rare:72 | ||||
| chr7:139341245-139341350 | Rare:18 | ||||
| chr7:139359692-139359968 | Common:2; Rare:113 | ||||
| chr7:141551284-141551423 | Common:1; Rare:43; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:141738192-141738464 | Rare:101 | ||||
| chr7:143407791-143407822 | Rare:2 | ||||
| chr7:143408821-143408961 | Rare:31 | ||||
| chr7:144355185-144355469 | Rare:2 | ||||
| chr7:149028602-149028967 | Common:4; Rare:124 | ||||
| chr7:150341587-150341836 | Common:2; Rare:30 |