| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66480239-66480450 | Common:1; Rare:56 | ||||
| chr11:66616364-66616638 | Common:1; Rare:79 | ||||
| chr11:66638393-66638725 | Common:3; Rare:146 | ||||
| chr11:67401778-67402075 | Common:3; Rare:111 | ||||
| chr11:67428394-67428531 | Rare:55 | ||||
| chr11:67443458-67443702 | Common:2; Rare:85 | ||||
| chr11:67482913-67483164 | Rare:56; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:67508606-67508945 | Common:4; Rare:101 | ||||
| chr11:68030381-68030737 | Common:3; Rare:100; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68271891-68272056 | Common:1; Rare:78 | ||||
| chr11:68903741-68903931 | Common:4; Rare:83; Clinvar (benign):6 | ||||
| chr11:69640972-69641272 | Common:1; Rare:66 | ||||
| chr11:69675309-69675541 | Common:1; Rare:64 | ||||
| chr11:70398455-70398596 | Common:1; Rare:46 | ||||
| chr11:71448306-71448720 | Common:5; Rare:109; Clinvar:3; Clinvar (benign):1 |