| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47248791-47248938 | Rare:59 | ||||
| chr11:47269545-47269811 | Common:1; Rare:93 | ||||
| chr11:47269972-47270184 | Common:1; Rare:71 | ||||
| chr11:47426412-47426648 | Rare:57 | ||||
| chr11:47565478-47565650 | Common:3; Rare:35 | ||||
| chr11:47578947-47579120 | Rare:91; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642443-47642830 | Rare:138 | ||||
| chr11:47767278-47767493 | Rare:90 | ||||
| chr11:57324883-57325181 | Common:1; Rare:98 | ||||
| chr11:57514851-57514970 | Rare:21 | ||||
| chr11:57530692-57530949 | Common:1; Rare:68 | ||||
| chr11:57567612-57567765 | Rare:49 | ||||
| chr11:57597605-57597731 | Rare:31; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:57712184-57712656 | Common:9; Rare:161 | ||||
| chr11:57741254-57741646 | Common:3; Rare:155 |