| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:172040384-172040616 | Common:1; Rare:55 | ||||
| chr3:172523352-172523595 | Common:1; Rare:64 | ||||
| chr3:172711010-172711122 | Rare:62 | ||||
| chr3:172711166-172711218 | Rare:9 | ||||
| chr3:172750546-172750763 | Common:3; Rare:65 | ||||
| chr3:174440682-174441018 | Common:3; Rare:86 | ||||
| chr3:177196411-177196540 | Rare:34 | ||||
| chr3:177197121-177197423 | Rare:103 | ||||
| chr3:179071540-179071899 | Rare:102 | ||||
| chr3:179147971-179148190 | Common:4; Rare:73 | ||||
| chr3:179347573-179347804 | Common:1; Rare:58 | ||||
| chr3:179604616-179604931 | Common:3; Rare:124 | ||||
| chr3:180602106-180602279 | Common:1; Rare:61 | ||||
| chr3:180912557-180912730 | Common:1; Rare:61 | ||||
| chr3:180989610-180989803 | Rare:83; Clinvar:1; Clinvar (benign):1 |