| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:129611600-129611762 | Common:2; Rare:48 | ||||
| chr7:131327777-131327894 | Rare:42 | ||||
| chr7:134646582-134646873 | Common:6; Rare:86 | ||||
| chr7:135170486-135170986 | Common:7; Rare:163 | ||||
| chr7:135662357-135662532 | Common:4; Rare:75 | ||||
| chr7:141551265-141551423 | Common:1; Rare:47; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:141738066-141738464 | Common:4; Rare:128 | ||||
| chr7:143380897-143381319 | Common:1; Rare:126 | ||||
| chr7:143902101-143902304 | Common:6; Rare:63 | ||||
| chr7:149126239-149126418 | Common:6; Rare:61 | ||||
| chr7:149873842-149873994 | Common:2; Rare:57 | ||||
| chr7:150379084-150379311 | Common:1; Rare:74 | ||||
| chr7:150800315-150800461 | Common:4; Rare:39 | ||||
| chr7:151080793-151080962 | Rare:51 | ||||
| chr7:151232371-151232528 | Common:1; Rare:53 |