| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52278639-52278781 | Rare:48 | ||||
| chr3:52287781-52287855 | Common:1; Rare:29 | ||||
| chr3:52455420-52455644 | Common:2; Rare:74 | ||||
| chr3:52536427-52536719 | Common:2; Rare:97 | ||||
| chr3:52685772-52686269 | Common:3; Rare:176 | ||||
| chr3:52705569-52706276 | Common:4; Rare:231 | ||||
| chr3:52770916-52771009 | Common:2; Rare:24 | ||||
| chr3:53130395-53130523 | Common:1; Rare:45; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:53347504-53347751 | Common:2; Rare:79 | ||||
| chr3:53891760-53892075 | Common:4; Rare:108 | ||||
| chr3:55481375-55481676 | Common:1; Rare:78 | ||||
| chr3:56557065-56557230 | Common:2; Rare:67 | ||||
| chr3:56977249-56977485 | Rare:45 | ||||
| chr3:57079252-57079388 | Common:2; Rare:45 | ||||
| chr3:57227654-57227901 | Common:3; Rare:80 |