| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65575847-65576090 | Common:3; Rare:70 | ||||
| chr11:65614179-65614335 | Rare:39 | ||||
| chr11:65615604-65615841 | Common:2; Rare:87 | ||||
| chr11:65642301-65642631 | Common:1; Rare:80 | ||||
| chr11:65662828-65663327 | Common:4; Rare:123 | ||||
| chr11:65711869-65712035 | Rare:51 | ||||
| chr11:65720445-65720579 | Common:1; Rare:73 | ||||
| chr11:65856936-65857369 | Common:4; Rare:132 | ||||
| chr11:65860182-65860459 | Common:1; Rare:93 | ||||
| chr11:65872681-65872960 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:65873550-65873694 | Common:2; Rare:46 | ||||
| chr11:65888333-65888670 | Common:1; Rare:107 | ||||
| chr11:65900367-65900589 | Common:1; Rare:44 | ||||
| chr11:65961498-65961773 | Common:1; Rare:95 | ||||
| chr11:66002108-66002392 | Common:3; Rare:85; Clinvar:4; Clinvar (benign):3 |