| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65524831-65525147 | Rare:55 | ||||
| chr11:65570422-65570504 | Rare:39 | ||||
| chr11:65662877-65663017 | Common:1; Rare:39 | ||||
| chr11:65663317-65663477 | Common:1; Rare:35 | ||||
| chr11:65860444-65860754 | Common:2; Rare:99 | ||||
| chr11:65872681-65872961 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:65888401-65888686 | Common:1; Rare:98 | ||||
| chr11:65900380-65900556 | Common:1; Rare:34 | ||||
| chr11:65919661-65920638 | Common:2; Rare:324 | ||||
| chr11:65961472-65961748 | Common:1; Rare:89 | ||||
| chr11:66002102-66002402 | Common:3; Rare:88; Clinvar:5; Clinvar (benign):3 | ||||
| chr11:66002456-66002819 | Common:1; Rare:101; Clinvar:1 | ||||
| chr11:66003514-66003737 | Common:1; Rare:72 | ||||
| chr11:66257577-66257785 | Rare:49 | ||||
| chr11:66268404-66268674 | Common:3; Rare:78 |