| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:160565284-160565842 | Common:3; Rare:187 | ||||
| chr3:160755456-160755677 | Common:1; Rare:81 | ||||
| chr3:167734837-167735254 | Common:5; Rare:132; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735626-167735752 | Rare:34 | ||||
| chr3:169769559-169769573 | Rare:6 | ||||
| chr3:169769581-169769616 | Rare:14 | ||||
| chr3:169773347-169773415 | Rare:20 | ||||
| chr3:169966632-169966858 | Common:2; Rare:89 | ||||
| chr3:172039491-172039683 | Common:1; Rare:67 | ||||
| chr3:172710989-172711343 | Common:1; Rare:112 | ||||
| chr3:172750539-172750747 | Common:3; Rare:61 | ||||
| chr3:174440912-174441006 | Common:1; Rare:25 | ||||
| chr3:179347595-179347936 | Common:1; Rare:88 | ||||
| chr3:179604581-179604932 | Common:4; Rare:144 | ||||
| chr3:180602100-180602235 | Common:1; Rare:44 |