| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65662877-65663275 | Common:3; Rare:97 | ||||
| chr11:65663298-65663477 | Common:2; Rare:42 | ||||
| chr11:65711877-65712039 | Rare:52 | ||||
| chr11:65720478-65720578 | Common:1; Rare:59 | ||||
| chr11:65856957-65857117 | Common:4; Rare:49 | ||||
| chr11:65860182-65860436 | Common:1; Rare:85 | ||||
| chr11:65860487-65860756 | Common:1; Rare:84 | ||||
| chr11:65872682-65872930 | Common:2; Rare:64; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:65873565-65873814 | Common:2; Rare:82 | ||||
| chr11:65888371-65888670 | Common:1; Rare:103 | ||||
| chr11:65961517-65961758 | Common:1; Rare:83 | ||||
| chr11:66002128-66002554 | Common:3; Rare:120; Clinvar:3; Clinvar (benign):3 | ||||
| chr11:66257578-66257842 | Rare:75 | ||||
| chr11:66268394-66268692 | Common:3; Rare:89 | ||||
| chr11:66289072-66289386 | Common:1; Rare:77 |