| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:73760267-73760328 | Rare:12 | ||||
| chr11:73760569-73760699 | Rare:32 | ||||
| chr11:73787828-73787986 | Common:1; Rare:48 | ||||
| chr11:73876618-73877068 | Common:5; Rare:138 | ||||
| chr11:74170830-74171437 | Common:4; Rare:194 | ||||
| chr11:74493137-74493409 | Common:1; Rare:100; Clinvar (pathogenic):1 | ||||
| chr11:74948995-74949371 | Common:8; Rare:117 | ||||
| chr11:75351662-75351807 | Common:2; Rare:43 | ||||
| chr11:75399397-75399595 | Common:4; Rare:85 | ||||
| chr11:75562694-75562883 | Common:1; Rare:43 | ||||
| chr11:75668611-75668928 | Rare:73 | ||||
| chr11:76381083-76381364 | Common:4; Rare:91 | ||||
| chr11:76444959-76445077 | Common:1; Rare:31 | ||||
| chr11:76783041-76783357 | Common:9; Rare:103 | ||||
| chr11:76783866-76784148 | Common:6; Rare:63 |