| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65720752-65721038 | Common:4; Rare:73; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:65833609-65833998 | Common:5; Rare:79 | ||||
| chr11:65857631-65857977 | Common:3; Rare:130 | ||||
| chr11:65859181-65859715 | Common:1; Rare:132 | ||||
| chr11:65860172-65860484 | Common:2; Rare:103 | ||||
| chr11:65888402-65888700 | Common:1; Rare:102 | ||||
| chr11:65890442-65890674 | Common:3; Rare:71 | ||||
| chr11:65920057-65920462 | Common:1; Rare:121 | ||||
| chr11:65961523-65961789 | Common:1; Rare:94 | ||||
| chr11:66002102-66002268 | Rare:49; Clinvar:4 | ||||
| chr11:66002456-66002818 | Common:1; Rare:101; Clinvar:1 | ||||
| chr11:66049105-66049355 | Common:2; Rare:48 | ||||
| chr11:66257154-66257289 | Rare:20 | ||||
| chr11:66257568-66257861 | Common:1; Rare:85 | ||||
| chr11:66258378-66258691 | Rare:86 |