| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:140941706-140941887 | Common:1; Rare:64 | ||||
| chr3:141231648-141231888 | Common:2; Rare:84 | ||||
| chr3:141368218-141368556 | Rare:72 | ||||
| chr3:142447985-142448130 | Common:1; Rare:48 | ||||
| chr3:149377628-149377937 | Common:1; Rare:60 | ||||
| chr3:149752459-149752598 | Common:2; Rare:42 | ||||
| chr3:150603162-150603342 | Common:2; Rare:68 | ||||
| chr3:152268687-152268963 | Rare:105 | ||||
| chr3:155854434-155854743 | Rare:80 | ||||
| chr3:155870308-155870718 | Common:2; Rare:122 | ||||
| chr3:156555077-156555419 | Common:2; Rare:122 | ||||
| chr3:156674356-156674635 | Common:3; Rare:82 | ||||
| chr3:157160112-157160284 | Rare:71 | ||||
| chr3:158105761-158105869 | Common:5; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:161221209-161221320 | Rare:31 |