| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:30606544-30606606 | Rare:20; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:31531867-31532427 | Common:9; Rare:181 | ||||
| chr3:31532519-31533061 | Common:5; Rare:207; Clinvar (benign):1 | ||||
| chr3:31533527-31533806 | Common:4; Rare:76 | ||||
| chr3:32106363-32106696 | Common:4; Rare:91; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32392164-32392445 | Common:4; Rare:57 | ||||
| chr3:32502220-32502419 | Common:1; Rare:43 | ||||
| chr3:32502742-32502956 | Rare:60 | ||||
| chr3:32570110-32570428 | Common:2; Rare:136 | ||||
| chr3:32570617-32571083 | Common:1; Rare:191 | ||||
| chr3:32684769-32684830 | Rare:8 | ||||
| chr3:32684965-32685403 | Rare:123 | ||||
| chr3:32817920-32818067 | Common:1; Rare:49 | ||||
| chr3:32951487-32951672 | Common:1; Rare:43 | ||||
| chr3:33096557-33096648 | Common:1; Rare:17 |