| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47214731-47215213 | Common:4; Rare:114; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47248782-47248970 | Rare:76 | ||||
| chr11:47472031-47472313 | Rare:57 | ||||
| chr11:47565500-47565674 | Common:3; Rare:36 | ||||
| chr11:47578928-47579334 | Rare:192; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr11:47638711-47639032 | Common:5; Rare:85 | ||||
| chr11:47767270-47767668 | Common:1; Rare:130 | ||||
| chr11:47848271-47848518 | Common:1; Rare:118 | ||||
| chr11:57324911-57325162 | Common:1; Rare:79 | ||||
| chr11:57530652-57531035 | Common:2; Rare:91 | ||||
| chr11:57567586-57567756 | Rare:58 | ||||
| chr11:57649878-57650059 | Common:1; Rare:46 | ||||
| chr11:57667697-57668028 | Common:5; Rare:97 | ||||
| chr11:57711968-57712630 | Common:10; Rare:218 | ||||
| chr11:57761704-57761895 | Rare:39 |