Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:128522165-128522521 | Common:1; Rare:106 | ||||
chr11:129279505-129279731 | Common:3; Rare:96 | ||||
chr11:129895535-129895666 | Common:2; Rare:48 | ||||
chr11:130002800-130002951 | Common:1; Rare:30 | ||||
chr11:130069551-130070018 | Common:2; Rare:174 | ||||
chr11:130314395-130314495 | Common:1; Rare:30 | ||||
chr11:130448401-130448668 | Rare:64 | ||||
chr11:130916403-130916682 | Common:6; Rare:86 | ||||
chr11:131911364-131911453 | Common:1; Rare:37 | ||||
chr11:133956771-133957116 | Common:2; Rare:106 | ||||
chr11:134224525-134224695 | Rare:64 | ||||
chr11:134225435-134225461 | Rare:8 | ||||
chr11:134253286-134253592 | Common:2; Rare:105; Clinvar (benign):1 | ||||
chr12:389229-389383 | Rare:60 | ||||
chr12:401438-401645 | Rare:57 |