| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52197970-52198171 | Common:1; Rare:85 | ||||
| chr3:52225587-52225838 | Rare:53 | ||||
| chr3:52239079-52239235 | Common:2; Rare:57 | ||||
| chr3:52278644-52278791 | Rare:50 | ||||
| chr3:52287759-52287859 | Common:2; Rare:41 | ||||
| chr3:52288023-52288085 | Rare:17 | ||||
| chr3:52410390-52410679 | Rare:64 | ||||
| chr3:52455385-52455653 | Common:2; Rare:85 | ||||
| chr3:52685949-52686095 | Common:2; Rare:62 | ||||
| chr3:52705787-52706249 | Common:2; Rare:166 | ||||
| chr3:52770911-52771036 | Common:2; Rare:28 | ||||
| chr3:53130398-53130568 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:53255963-53256174 | Common:2; Rare:91 | ||||
| chr3:53347518-53347734 | Common:1; Rare:68 | ||||
| chr3:53882116-53882328 | Common:3; Rare:77 |