| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65614216-65614420 | Rare:41 | ||||
| chr11:65638011-65638180 | Common:3; Rare:75 | ||||
| chr11:65662895-65663099 | Common:1; Rare:50 | ||||
| chr11:65712156-65712270 | Rare:44 | ||||
| chr11:65720439-65720578 | Common:1; Rare:73 | ||||
| chr11:65860338-65860452 | Common:1; Rare:34 | ||||
| chr11:65873570-65873722 | Common:2; Rare:48 | ||||
| chr11:65888426-65888692 | Common:1; Rare:92 | ||||
| chr11:65961517-65961742 | Common:1; Rare:74 | ||||
| chr11:66002105-66002812 | Common:4; Rare:200; Clinvar:6; Clinvar (benign):3 | ||||
| chr11:66257568-66257773 | Rare:49 | ||||
| chr11:66268394-66268659 | Common:3; Rare:79 | ||||
| chr11:66289072-66289393 | Common:1; Rare:77 | ||||
| chr11:66345049-66345216 | Common:1; Rare:46 | ||||
| chr11:66371737-66371924 | Common:1; Rare:47 |