| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:73876773-73877036 | Common:5; Rare:75 | ||||
| chr11:74170814-74171441 | Common:4; Rare:197 | ||||
| chr11:74949039-74949319 | Common:6; Rare:82 | ||||
| chr11:76381100-76381364 | Common:4; Rare:83 | ||||
| chr11:76444598-76445053 | Common:1; Rare:111 | ||||
| chr11:76783060-76783388 | Common:10; Rare:106 | ||||
| chr11:77473550-77473791 | Common:1; Rare:90 | ||||
| chr11:77589531-77589595 | Rare:28 | ||||
| chr11:77637703-77637877 | Common:1; Rare:62 | ||||
| chr11:77820989-77821210 | Common:1; Rare:68 | ||||
| chr11:78079751-78079961 | Common:2; Rare:64 | ||||
| chr11:78139590-78139779 | Common:3; Rare:76; Clinvar:2 | ||||
| chr11:78574773-78574934 | Common:2; Rare:64; Clinvar (benign):1 | ||||
| chr11:83071797-83072111 | Common:4; Rare:89 | ||||
| chr11:83193621-83193786 | Common:1; Rare:75 |