| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:57427593-57427929 | Common:3; Rare:52 | ||||
| chr11:57514858-57514938 | Rare:10 | ||||
| chr11:57515695-57515964 | Common:1; Rare:50 | ||||
| chr11:57530682-57530843 | Common:1; Rare:41 | ||||
| chr11:57567604-57567777 | Rare:54 | ||||
| chr11:57597172-57597737 | Rare:110; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:57606003-57606547 | Rare:146; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:57657434-57657812 | Common:4; Rare:94 | ||||
| chr11:57711997-57712048 | Common:1; Rare:17 | ||||
| chr11:57712175-57712665 | Common:9; Rare:169 | ||||
| chr11:57741372-57741609 | Rare:93 | ||||
| chr11:58578008-58578197 | Rare:55 | ||||
| chr11:58578335-58578508 | Common:2; Rare:63 | ||||
| chr11:58578902-58579192 | Common:4; Rare:77 | ||||
| chr11:58731934-58732013 | Rare:13 |