| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65900322-65900479 | Common:3; Rare:31 | ||||
| chr11:65900546-65900792 | Common:3; Rare:53 | ||||
| chr11:65961628-65961783 | Rare:54 | ||||
| chr11:66002097-66002287 | Common:1; Rare:59; Clinvar:5; Clinvar (benign):1 | ||||
| chr11:66002466-66002838 | Common:1; Rare:104; Clinvar:1 | ||||
| chr11:66011952-66012278 | Common:2; Rare:104 | ||||
| chr11:66058054-66058405 | Rare:88 | ||||
| chr11:66257559-66257865 | Common:1; Rare:89 | ||||
| chr11:66268382-66268682 | Common:3; Rare:91 | ||||
| chr11:66289086-66289398 | Common:1; Rare:73 | ||||
| chr11:66344972-66345203 | Common:1; Rare:63 | ||||
| chr11:66347622-66347898 | Common:5; Rare:66 | ||||
| chr11:66480228-66480453 | Common:1; Rare:59 | ||||
| chr11:66519416-66519643 | Common:1; Rare:41; Clinvar (benign):2 | ||||
| chr11:66593078-66593253 | Common:1; Rare:64 |