| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:150800296-150800860 | Common:9; Rare:145 | ||||
| chr7:150801346-150801693 | Common:5; Rare:111 | ||||
| chr7:150852222-150852537 | Common:3; Rare:46 | ||||
| chr7:151028206-151028507 | Rare:120 | ||||
| chr7:151080793-151080920 | Rare:41 | ||||
| chr7:151232408-151232500 | Rare:21 | ||||
| chr7:151408988-151409311 | Common:1; Rare:84 | ||||
| chr7:152025583-152025775 | Rare:78 | ||||
| chr7:152078881-152079020 | Common:2; Rare:26 | ||||
| chr7:152676096-152676276 | Common:2; Rare:71; Clinvar (benign):6 | ||||
| chr7:155644320-155644724 | Common:2; Rare:136 | ||||
| chr7:156640547-156640700 | Common:3; Rare:80 | ||||
| chr7:157336776-157337124 | Common:3; Rare:166; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:158856392-158856716 | Common:7; Rare:109 | ||||
| chr8:232122-232480 | Common:3; Rare:147 |