| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47426416-47426660 | Rare:58 | ||||
| chr11:47565478-47565667 | Common:3; Rare:40 | ||||
| chr11:47578959-47579118 | Rare:84; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47767301-47767428 | Rare:58 | ||||
| chr11:57324860-57325162 | Common:2; Rare:98 | ||||
| chr11:57427049-57427221 | Common:1; Rare:55 | ||||
| chr11:57514851-57514977 | Rare:22 | ||||
| chr11:57567612-57567915 | Common:2; Rare:84 | ||||
| chr11:57606000-57606502 | Rare:139; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:57712178-57712676 | Common:9; Rare:174 | ||||
| chr11:57741290-57741596 | Common:1; Rare:116 | ||||
| chr11:58578095-58578168 | Rare:21 | ||||
| chr11:58578346-58578508 | Common:2; Rare:61 | ||||
| chr11:58578855-58579237 | Common:5; Rare:110 | ||||
| chr11:59142667-59142945 | Common:1; Rare:50 |