| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46936646-46936808 | Common:2; Rare:50 | ||||
| chr11:47176837-47177099 | Common:1; Rare:110 | ||||
| chr11:47186365-47186544 | Rare:53 | ||||
| chr11:47214834-47215127 | Common:2; Rare:80; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47248785-47248957 | Rare:71 | ||||
| chr11:47269083-47269382 | Common:1; Rare:60 | ||||
| chr11:47269550-47269711 | Common:1; Rare:53 | ||||
| chr11:47269972-47270203 | Common:1; Rare:83 | ||||
| chr11:47426363-47426663 | Common:1; Rare:76 | ||||
| chr11:47553024-47553372 | Common:2; Rare:121 | ||||
| chr11:47565478-47565661 | Common:3; Rare:39 | ||||
| chr11:47578654-47579136 | Common:1; Rare:172; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47594409-47594522 | Common:1; Rare:33 | ||||
| chr11:47642447-47642793 | Rare:128 | ||||
| chr11:47767305-47767679 | Common:1; Rare:115 |