| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:83682714-83682759 | Rare:3 | ||||
| chr11:83724918-83725026 | Rare:26 | ||||
| chr11:83725255-83725427 | Rare:29 | ||||
| chr11:85627811-85627872 | Rare:9 | ||||
| chr11:85628157-85628222 | Rare:16 | ||||
| chr11:85628283-85628674 | Common:8; Rare:129 | ||||
| chr11:85628832-85628845 | Rare:1 | ||||
| chr11:85629051-85629149 | Rare:34 | ||||
| chr11:85647696-85648194 | Common:3; Rare:126; Clinvar:3; Clinvar (benign):3 | ||||
| chr11:85648228-85648252 | Rare:5 | ||||
| chr11:85648401-85648510 | Rare:24 | ||||
| chr11:85663686-85663990 | Common:1; Rare:86 | ||||
| chr11:85664150-85664650 | Common:2; Rare:194 | ||||
| chr11:85664656-85664890 | Common:1; Rare:106 | ||||
| chr11:85665014-85665307 | Common:1; Rare:107 |