| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52705576-52706227 | Common:4; Rare:208 | ||||
| chr3:52834856-52835030 | Common:1; Rare:49 | ||||
| chr3:52897358-52897668 | Rare:93 | ||||
| chr3:53130405-53130556 | Common:1; Rare:48; Clinvar (benign):3 | ||||
| chr3:53255896-53256174 | Common:3; Rare:104 | ||||
| chr3:53347504-53347741 | Common:2; Rare:76 | ||||
| chr3:53891784-53892021 | Common:2; Rare:75 | ||||
| chr3:56557065-56557230 | Common:2; Rare:67 | ||||
| chr3:57079247-57079389 | Common:2; Rare:46 | ||||
| chr3:57227600-57227922 | Common:4; Rare:107 | ||||
| chr3:57556000-57556321 | Rare:80 | ||||
| chr3:57597331-57597778 | Common:4; Rare:131 | ||||
| chr3:57756219-57756324 | Rare:29 | ||||
| chr3:57889771-57890129 | Common:1; Rare:72; Clinvar (benign):2 | ||||
| chr3:58433799-58433923 | Rare:48; Clinvar (benign):3 |