| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:143380978-143381312 | Common:1; Rare:103 | ||||
| chr7:143382097-143382452 | Common:1; Rare:121 | ||||
| chr7:143902122-143902304 | Common:5; Rare:58 | ||||
| chr7:144835994-144836053 | Rare:12 | ||||
| chr7:149028642-149028911 | Common:1; Rare:87 | ||||
| chr7:149090705-149090897 | Rare:49 | ||||
| chr7:150737241-150737439 | Common:3; Rare:35 | ||||
| chr7:150993566-150993783 | Rare:56 | ||||
| chr7:151013774-151014058 | Common:1; Rare:122; Clinvar (benign):1 | ||||
| chr7:151028158-151028487 | Rare:116 | ||||
| chr7:151080793-151080940 | Rare:44 | ||||
| chr7:151227158-151227435 | Common:1; Rare:74 | ||||
| chr7:152025583-152025789 | Rare:84 | ||||
| chr7:155644384-155644751 | Common:2; Rare:122 | ||||
| chr7:156640554-156640685 | Common:2; Rare:68 |