| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52705576-52706227 | Common:4; Rare:208 | ||||
| chr3:52770916-52771028 | Common:2; Rare:27 | ||||
| chr3:53255834-53255875 | Rare:7 | ||||
| chr3:53255938-53256163 | Common:3; Rare:90 | ||||
| chr3:53347504-53347734 | Common:2; Rare:74 | ||||
| chr3:53891816-53892075 | Common:4; Rare:86 | ||||
| chr3:56557086-56557234 | Common:2; Rare:58 | ||||
| chr3:56682884-56682935 | Common:2; Rare:16 | ||||
| chr3:57079257-57079388 | Common:2; Rare:42 | ||||
| chr3:57165288-57165577 | Common:1; Rare:87 | ||||
| chr3:57227585-57227889 | Common:3; Rare:105 | ||||
| chr3:57555979-57556339 | Rare:92 | ||||
| chr3:57597333-57597778 | Common:4; Rare:131 | ||||
| chr3:58306093-58306328 | Common:1; Rare:65 | ||||
| chr3:58433766-58434043 | Common:2; Rare:108; Clinvar:2; Clinvar (benign):3 |