| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:128693803-128693919 | Common:2; Rare:25 | ||||
| chr11:128693966-128694195 | Rare:41 | ||||
| chr11:129279509-129279752 | Common:3; Rare:108 | ||||
| chr11:129895529-129895687 | Common:2; Rare:62 | ||||
| chr11:130002776-130002973 | Common:3; Rare:37 | ||||
| chr11:130916394-130916627 | Common:7; Rare:76 | ||||
| chr11:131909441-131909934 | Common:7; Rare:79 | ||||
| chr11:131911306-131911626 | Common:2; Rare:110 | ||||
| chr11:134224537-134224690 | Rare:57 | ||||
| chr11:134253276-134253601 | Common:2; Rare:113; Clinvar (benign):1 | ||||
| chr12:389249-389383 | Rare:51 | ||||
| chr12:389512-389667 | Common:5; Rare:66 | ||||
| chr12:401438-401669 | Rare:64 | ||||
| chr12:752314-752587 | Common:1; Rare:81 | ||||
| chr12:949626-949844 | Common:4; Rare:66 |