| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:506398-506462 | Common:2; Rare:13 | ||||
| chr11:506607-506629 | Rare:8 | ||||
| chr11:506726-507005 | Common:3; Rare:93 | ||||
| chr11:507118-507576 | Common:4; Rare:149 | ||||
| chr11:537303-537532 | Common:5; Rare:71 | ||||
| chr11:560701-561016 | Common:6; Rare:146 | ||||
| chr11:576412-576531 | Rare:48 | ||||
| chr11:615627-616033 | Common:3; Rare:134 | ||||
| chr11:695614-695833 | Rare:55 | ||||
| chr11:706928-707310 | Common:3; Rare:87 | ||||
| chr11:747290-747587 | Rare:125; Clinvar:5; Clinvar (benign):1 | ||||
| chr11:755758-756002 | Rare:86; Clinvar:2 | ||||
| chr11:763338-763968 | Rare:273; Clinvar:5; Clinvar (pathogenic):3 | ||||
| chr11:764030-764430 | Common:2; Rare:110; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:777447-777619 | Common:1; Rare:78 |