Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:126304224-126304412 | Common:3; Rare:66 | ||||
chr11:126355526-126355742 | Common:2; Rare:56 | ||||
chr11:127003314-127003460 | Common:2; Rare:34 | ||||
chr11:129279491-129279787 | Common:5; Rare:126 | ||||
chr11:129895509-129895682 | Common:2; Rare:72 | ||||
chr11:130002504-130002629 | Rare:29 | ||||
chr11:130002736-130002951 | Common:2; Rare:44 | ||||
chr11:130003006-130003304 | Common:1; Rare:115 | ||||
chr11:130069532-130069940 | Common:2; Rare:153 | ||||
chr11:130314395-130314472 | Rare:29 | ||||
chr11:130916394-130916648 | Common:7; Rare:78 | ||||
chr11:131911178-131911219 | Rare:17 | ||||
chr11:131911339-131911502 | Common:1; Rare:65 | ||||
chr11:134068864-134069094 | Rare:109; Clinvar (pathogenic):1 | ||||
chr11:134223924-134224166 | Common:2; Rare:79 |