| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:9003986-9004122 | Rare:54 | ||||
| chr11:9460719-9461018 | Common:3; Rare:84 | ||||
| chr11:9664000-9664164 | Common:4; Rare:55 | ||||
| chr11:10304805-10305085 | Common:1; Rare:61 | ||||
| chr11:10541141-10541324 | Rare:70 | ||||
| chr11:10802142-10802384 | Common:1; Rare:68 | ||||
| chr11:10858023-10858241 | Common:2; Rare:63 | ||||
| chr11:11841941-11842016 | Common:1; Rare:25 | ||||
| chr11:12377459-12377633 | Rare:69 | ||||
| chr11:13463162-13463346 | Common:1; Rare:65 | ||||
| chr11:18322109-18322288 | Common:3; Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322474-18322724 | Common:2; Rare:90 | ||||
| chr11:18526880-18526991 | Rare:50 | ||||
| chr11:18588653-18588902 | Common:2; Rare:90 | ||||
| chr11:27506718-27506859 | Common:1; Rare:67 |