| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:53130405-53130533 | Common:1; Rare:40; Clinvar (benign):3 | ||||
| chr3:53347525-53347734 | Common:1; Rare:64 | ||||
| chr3:53891813-53892075 | Common:4; Rare:86 | ||||
| chr3:56557076-56557221 | Common:2; Rare:54 | ||||
| chr3:57079257-57079388 | Common:2; Rare:42 | ||||
| chr3:57227609-57227821 | Common:2; Rare:72 | ||||
| chr3:57556012-57556321 | Rare:75 | ||||
| chr3:57597326-57597661 | Common:4; Rare:106 | ||||
| chr3:58332646-58332916 | Common:9; Rare:60 | ||||
| chr3:67654593-67654722 | Common:1; Rare:46 | ||||
| chr3:69013662-69013968 | Common:2; Rare:105 | ||||
| chr3:72996712-72997030 | Common:2; Rare:119 | ||||
| chr3:87227217-87227375 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:88058953-88059282 | Common:2; Rare:110 | ||||
| chr3:94062920-94063011 | Rare:28 |