| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:152243320-152243998 | Common:7; Rare:268 | ||||
| chr3:152244252-152244652 | Common:5; Rare:79 | ||||
| chr3:152268057-152268457 | Common:2; Rare:93 | ||||
| chr3:152268410-152269140 | Common:10; Rare:1081; Clinvar (benign):2 | ||||
| chr3:152269134-152269439 | Rare:149 | ||||
| chr3:152269405-152270422 | Common:24; Rare:788 | ||||
| chr3:152298951-152299926 | Common:3; Rare:311 | ||||
| chr3:152833647-152835240 | Common:47; Rare:993 | ||||
| chr3:153161922-153162739 | Common:4; Rare:768 | ||||
| chr3:154121090-154121555 | Common:13; Rare:499 | ||||
| chr3:154324360-154324690 | Rare:501 | ||||
| chr3:154324943-154325343 | Common:2; Rare:63 | ||||
| chr3:155079350-155080137 | Common:27; Rare:467 | ||||
| chr3:155080111-155080511 | Common:3; Rare:111 | ||||
| chr3:155744217-155745089 | Common:2; Rare:518 |