| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65614014-65614339 | Rare:77 | ||||
| chr11:65645616-65645946 | Rare:73 | ||||
| chr11:65650241-65650454 | Rare:65 | ||||
| chr11:65662886-65663081 | Common:1; Rare:50 | ||||
| chr11:65720457-65720578 | Common:1; Rare:69 | ||||
| chr11:65833769-65833970 | Rare:44 | ||||
| chr11:65860178-65860441 | Common:1; Rare:87 | ||||
| chr11:65868022-65868308 | Common:2; Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:65890468-65890730 | Common:4; Rare:86 | ||||
| chr11:65920340-65920647 | Rare:104 | ||||
| chr11:65961517-65961784 | Common:1; Rare:95 | ||||
| chr11:66002097-66002564 | Common:3; Rare:134; Clinvar:7; Clinvar (benign):3 | ||||
| chr11:66257613-66257773 | Rare:37 | ||||
| chr11:66341582-66341861 | Common:1; Rare:83 | ||||
| chr11:66347626-66347845 | Common:5; Rare:52 |