| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18394413-18394641 | Common:1; Rare:87; Clinvar (benign):1 | ||||
| chr11:18526782-18526993 | Common:1; Rare:93 | ||||
| chr11:18588667-18588929 | Common:3; Rare:86 | ||||
| chr11:18634246-18634588 | Common:3; Rare:120 | ||||
| chr11:20022992-20023046 | Rare:10 | ||||
| chr11:20363669-20363801 | Common:3; Rare:27 | ||||
| chr11:20364093-20364186 | Rare:23 | ||||
| chr11:20387392-20387786 | Common:8; Rare:127 | ||||
| chr11:22625499-22625622 | Rare:62; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625808-22626021 | Common:3; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:22666905-22667144 | Common:1; Rare:65 | ||||
| chr11:22674590-22674898 | Common:3; Rare:52 | ||||
| chr11:22829357-22829422 | Common:1; Rare:18 | ||||
| chr11:27506721-27506877 | Common:1; Rare:72 | ||||
| chr11:28108104-28108414 | Common:1; Rare:92 |