| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47270012-47270211 | Common:1; Rare:74 | ||||
| chr11:47565496-47565643 | Common:3; Rare:28 | ||||
| chr11:47578952-47579089 | Rare:70; Clinvar:2 | ||||
| chr11:47642467-47642815 | Rare:129 | ||||
| chr11:47767247-47767470 | Common:1; Rare:95 | ||||
| chr11:57311438-57311724 | Common:1; Rare:75 | ||||
| chr11:57324883-57325173 | Common:1; Rare:96 | ||||
| chr11:57427028-57427257 | Common:1; Rare:70 | ||||
| chr11:57597573-57597744 | Rare:43; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:57657555-57657796 | Common:3; Rare:58 | ||||
| chr11:57712175-57712637 | Common:9; Rare:156 | ||||
| chr11:57741257-57741589 | Common:1; Rare:127 | ||||
| chr11:58578101-58578546 | Common:4; Rare:140 | ||||
| chr11:58578889-58579231 | Common:5; Rare:94 | ||||
| chr11:59142689-59142945 | Common:1; Rare:45 |