| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34052159-34052510 | Common:4; Rare:160 | ||||
| chr11:34105478-34105724 | Common:2; Rare:82 | ||||
| chr11:34438769-34438985 | Common:1; Rare:71 | ||||
| chr11:34916294-34916661 | Common:10; Rare:149; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35943949-35944128 | Common:2; Rare:65 | ||||
| chr11:36289378-36289539 | Common:2; Rare:60 | ||||
| chr11:36510240-36510361 | Rare:34 | ||||
| chr11:43311758-43312053 | Common:2; Rare:96 | ||||
| chr11:43358794-43358979 | Rare:89 | ||||
| chr11:43359170-43359258 | Rare:24 | ||||
| chr11:43880663-43880884 | Common:2; Rare:52 | ||||
| chr11:45918796-45918876 | Rare:21 | ||||
| chr11:46594006-46594095 | Rare:20 | ||||
| chr11:46617173-46617572 | Common:5; Rare:114 | ||||
| chr11:46700544-46700925 | Common:1; Rare:92 |