| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65662837-65663028 | Common:1; Rare:50 | ||||
| chr11:65663324-65663489 | Common:1; Rare:37 | ||||
| chr11:65711869-65712051 | Rare:59 | ||||
| chr11:65712169-65712270 | Rare:39 | ||||
| chr11:65856988-65857329 | Common:4; Rare:102 | ||||
| chr11:65860157-65860832 | Common:3; Rare:222 | ||||
| chr11:65873557-65873722 | Common:3; Rare:50 | ||||
| chr11:65888374-65888686 | Common:1; Rare:105 | ||||
| chr11:65890495-65890690 | Common:3; Rare:66 | ||||
| chr11:65900322-65900455 | Common:3; Rare:24 | ||||
| chr11:65961498-65961773 | Common:1; Rare:95 | ||||
| chr11:66002078-66002402 | Common:3; Rare:94; Clinvar:7; Clinvar (benign):3 | ||||
| chr11:66002422-66002845 | Common:1; Rare:119; Clinvar:1 | ||||
| chr11:66268404-66268671 | Common:3; Rare:78 | ||||
| chr11:66288975-66289393 | Common:2; Rare:105 |