| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52705565-52706276 | Common:4; Rare:233 | ||||
| chr3:52770905-52771009 | Common:2; Rare:29 | ||||
| chr3:53130388-53130541 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:53255919-53256149 | Common:2; Rare:89 | ||||
| chr3:53347518-53347734 | Common:1; Rare:68 | ||||
| chr3:53493994-53494266 | Common:5; Rare:80 | ||||
| chr3:53846420-53846573 | Rare:50 | ||||
| chr3:53891791-53892088 | Common:5; Rare:99 | ||||
| chr3:56557081-56557234 | Common:2; Rare:59 | ||||
| chr3:56682815-56683070 | Common:2; Rare:105 | ||||
| chr3:56683099-56683325 | Common:4; Rare:78 | ||||
| chr3:57079243-57079404 | Common:2; Rare:52 | ||||
| chr3:57227585-57227922 | Common:4; Rare:114 | ||||
| chr3:57555996-57556321 | Rare:81 | ||||
| chr3:57597278-57597799 | Common:7; Rare:157 |