| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12994718-12994797 | Rare:12 | ||||
| chr3:13420208-13420426 | Common:1; Rare:65 | ||||
| chr3:13480033-13480334 | Common:2; Rare:71 | ||||
| chr3:14124673-14125179 | Common:4; Rare:150; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178532-14178881 | Common:2; Rare:181; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402415-14402749 | Common:4; Rare:76 | ||||
| chr3:14651486-14651818 | Rare:98 | ||||
| chr3:14947222-14947583 | Common:4; Rare:161 | ||||
| chr3:14948407-14948637 | Common:2; Rare:63 | ||||
| chr3:15065219-15065364 | Common:2; Rare:59 | ||||
| chr3:15099119-15099304 | Rare:46 | ||||
| chr3:15206008-15206290 | Common:1; Rare:105 | ||||
| chr3:15332269-15332286 | Rare:2 | ||||
| chr3:15332393-15332715 | Common:3; Rare:98 | ||||
| chr3:15333248-15333441 | Rare:28 |