| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:138174855-138174958 | Common:1; Rare:21 | ||||
| chr3:138834858-138835066 | Rare:75 | ||||
| chr3:139389552-139389878 | Common:2; Rare:105 | ||||
| chr3:139539468-139539758 | Common:3; Rare:99 | ||||
| chr3:141231652-141231888 | Common:2; Rare:83 | ||||
| chr3:141402267-141402417 | Common:2; Rare:44 | ||||
| chr3:141876452-141876652 | Common:1; Rare:74 | ||||
| chr3:142225538-142225637 | Common:1; Rare:31 | ||||
| chr3:142447872-142448130 | Common:1; Rare:71 | ||||
| chr3:142578700-142578926 | Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:142961729-142961924 | Common:2; Rare:24 | ||||
| chr3:142962274-142962570 | Common:1; Rare:74 | ||||
| chr3:142962765-142962957 | Common:1; Rare:60 | ||||
| chr3:142963838-142964082 | Common:4; Rare:64 | ||||
| chr3:143001466-143001640 | Common:2; Rare:62 |