| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52287749-52287859 | Common:2; Rare:46 | ||||
| chr3:52289783-52290101 | Rare:48 | ||||
| chr3:52455424-52455657 | Common:2; Rare:80 | ||||
| chr3:52525024-52525371 | Common:9; Rare:149 | ||||
| chr3:52536377-52536703 | Common:2; Rare:106 | ||||
| chr3:52685544-52686093 | Common:4; Rare:180 | ||||
| chr3:52705558-52706279 | Common:4; Rare:238 | ||||
| chr3:53130405-53130657 | Common:1; Rare:85; Clinvar (benign):3 | ||||
| chr3:53347518-53347734 | Common:1; Rare:68 | ||||
| chr3:53891794-53892035 | Common:2; Rare:72 | ||||
| chr3:54928013-54928016 | |||||
| chr3:55481375-55481444 | Rare:19 | ||||
| chr3:56557081-56557238 | Common:2; Rare:61 | ||||
| chr3:56776058-56776261 | Rare:36 | ||||
| chr3:56801875-56802078 | Rare:71 |