| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47269972-47270184 | Common:1; Rare:71 | ||||
| chr11:47426412-47426648 | Rare:57 | ||||
| chr11:47553071-47553347 | Common:2; Rare:101 | ||||
| chr11:47565517-47565650 | Common:2; Rare:25 | ||||
| chr11:47578947-47579097 | Rare:77; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642452-47642705 | Rare:102 | ||||
| chr11:47767278-47767501 | Rare:92 | ||||
| chr11:57311450-57311669 | Common:1; Rare:55 | ||||
| chr11:57335740-57335926 | Common:4; Rare:45 | ||||
| chr11:57514858-57514970 | Rare:20 | ||||
| chr11:57530681-57530809 | Rare:34 | ||||
| chr11:57567612-57567840 | Rare:69 | ||||
| chr11:57657428-57657801 | Common:4; Rare:95 | ||||
| chr11:57667725-57668041 | Common:5; Rare:95 | ||||
| chr11:57711972-57712635 | Common:10; Rare:220 |