| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126303989-126304073 | Rare:48 | ||||
| chr11:126355531-126355713 | Common:1; Rare:43 | ||||
| chr11:129895535-129895666 | Common:2; Rare:48 | ||||
| chr11:130069630-130070079 | Common:2; Rare:159 | ||||
| chr11:130314390-130314475 | Rare:30 | ||||
| chr11:130916437-130916631 | Common:5; Rare:59 | ||||
| chr11:131911364-131911492 | Common:1; Rare:56 | ||||
| chr11:134223930-134224122 | Common:2; Rare:56 | ||||
| chr11:134253306-134253594 | Common:2; Rare:94; Clinvar (benign):1 | ||||
| chr12:389230-389383 | Rare:60 | ||||
| chr12:389544-389656 | Common:5; Rare:54 | ||||
| chr12:401446-401664 | Rare:58 | ||||
| chr12:752301-752587 | Common:1; Rare:87 | ||||
| chr12:991101-991318 | Common:3; Rare:99 | ||||
| chr12:2004427-2004645 | Common:1; Rare:72 |