| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:130916370-130916770 | Common:20; Rare:266 | ||||
| chr11:134223851-134224251 | Common:12; Rare:575 | ||||
| chr11:134224407-134224807 | Common:6; Rare:648 | ||||
| chr11:134224840-134225454 | Common:10; Rare:446 | ||||
| chr11:134225432-134225563 | Rare:69 | ||||
| chr11:134234655-134235055 | Common:2; Rare:132 | ||||
| chr11:134252746-134253146 | Common:1; Rare:152 | ||||
| chr11:134253242-134253642 | Common:13; Rare:618; Clinvar:1; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr11:134275979-134276490 | Common:8; Rare:143 | ||||
| chr11:134331451-134332215 | Common:42; Rare:450 | ||||
| chr11:134332259-134332659 | Common:1; Rare:107 | ||||
| chr11:134355285-134356045 | Common:5; Rare:341 | ||||
| chr11:134412020-134412410 | Common:2; Rare:110 | ||||
| chr12:199853-199956 | Rare:19 | ||||
| chr12:262634-263134 | Common:2; Rare:276 |