| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:20363651-20363753 | Common:2; Rare:22 | ||||
| chr11:20364102-20364287 | Rare:57 | ||||
| chr11:20387475-20387777 | Common:5; Rare:97 | ||||
| chr11:22624972-22625244 | Common:3; Rare:106; Clinvar:5; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr11:22625515-22625609 | Rare:47; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625802-22626021 | Common:3; Rare:73; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:22829357-22829440 | Common:1; Rare:24 | ||||
| chr11:26994022-26994128 | Rare:15 | ||||
| chr11:27506725-27506864 | Common:1; Rare:64 | ||||
| chr11:28108115-28108414 | Common:1; Rare:90 | ||||
| chr11:30322971-30323175 | Common:1; Rare:60 | ||||
| chr11:31369737-31369882 | Rare:45 | ||||
| chr11:31509567-31509911 | Common:1; Rare:123 | ||||
| chr11:32435536-32435613 | Common:1; Rare:12 | ||||
| chr11:32435614-32435839 | Rare:72 |