| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:170038035-170038201 | Common:4; Rare:41 | ||||
| chr3:170181223-170181304 | Rare:26 | ||||
| chr3:170870138-170870283 | Rare:85 | ||||
| chr3:170908572-170908827 | Common:1; Rare:70 | ||||
| chr3:172523352-172523592 | Common:1; Rare:63 | ||||
| chr3:172711051-172711208 | Rare:59 | ||||
| chr3:172750581-172750794 | Common:3; Rare:61 | ||||
| chr3:174440912-174441001 | Common:1; Rare:25 | ||||
| chr3:179148028-179148196 | Common:3; Rare:60 | ||||
| chr3:179347583-179347799 | Common:1; Rare:51 | ||||
| chr3:179604594-179604911 | Common:3; Rare:134 | ||||
| chr3:180602032-180602262 | Common:1; Rare:83 | ||||
| chr3:180912557-180912730 | Common:1; Rare:61 | ||||
| chr3:180989618-180989820 | Rare:87; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:181711730-181712047 | Rare:86 |