| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:172523352-172523598 | Common:1; Rare:65 | ||||
| chr3:172750565-172750787 | Common:3; Rare:64 | ||||
| chr3:177196398-177196563 | Rare:49 | ||||
| chr3:177197212-177197413 | Rare:70 | ||||
| chr3:179071576-179071908 | Rare:94 | ||||
| chr3:179147970-179148196 | Common:4; Rare:74 | ||||
| chr3:179347545-179347799 | Common:2; Rare:60 | ||||
| chr3:179604600-179604929 | Common:3; Rare:135 | ||||
| chr3:180602032-180602366 | Common:1; Rare:114 | ||||
| chr3:180602449-180602584 | Rare:37 | ||||
| chr3:180989647-180989838 | Rare:77; Clinvar:1 | ||||
| chr3:182793334-182793718 | Common:3; Rare:114 | ||||
| chr3:183099433-183099742 | Common:2; Rare:102; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr3:183252948-183253353 | Common:4; Rare:104 | ||||
| chr3:183555603-183555826 | Common:1; Rare:61 |