| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:170908570-170908843 | Common:1; Rare:77 | ||||
| chr3:171460100-171460209 | Rare:27 | ||||
| chr3:171460214-171460532 | Common:2; Rare:70 | ||||
| chr3:171460769-171460987 | Common:1; Rare:57 | ||||
| chr3:172750546-172750763 | Common:3; Rare:65 | ||||
| chr3:173397478-173397820 | Common:4; Rare:112 | ||||
| chr3:177196465-177196782 | Common:2; Rare:106 | ||||
| chr3:179347545-179347804 | Common:2; Rare:64 | ||||
| chr3:179604610-179604848 | Common:2; Rare:88 | ||||
| chr3:180601994-180602269 | Common:1; Rare:93 | ||||
| chr3:180989618-180989838 | Rare:91; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:183697673-183697909 | Common:2; Rare:107 | ||||
| chr3:183884817-183884947 | Rare:56 | ||||
| chr3:184017876-184018073 | Common:1; Rare:58 | ||||
| chr3:184135221-184135403 | Common:2; Rare:56; Clinvar:5 |