| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126355532-126355742 | Common:1; Rare:54 | ||||
| chr11:129895509-129895708 | Common:3; Rare:78 | ||||
| chr11:130069624-130069990 | Common:2; Rare:131 | ||||
| chr11:130314395-130314495 | Common:1; Rare:30 | ||||
| chr11:130448422-130448652 | Rare:54 | ||||
| chr11:130916421-130916648 | Common:5; Rare:70 | ||||
| chr11:133532351-133532452 | Common:1; Rare:18 | ||||
| chr11:133957000-133957105 | Common:1; Rare:35 | ||||
| chr11:134223922-134224166 | Common:2; Rare:80 | ||||
| chr11:134253234-134253608 | Common:2; Rare:126; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:134276195-134276362 | Common:3; Rare:35 | ||||
| chr12:389221-389354 | Rare:50 | ||||
| chr12:389539-389635 | Common:5; Rare:43 | ||||
| chr12:401446-401685 | Rare:65 | ||||
| chr12:752306-752587 | Common:1; Rare:85 |