Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:111631137-111631369 | Common:1; Rare:64 | ||||
chr9:112379834-112380116 | Common:3; Rare:109 | ||||
chr9:113221270-113221621 | Rare:106 | ||||
chr9:116687203-116687364 | Common:3; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
chr9:121370231-121370467 | Common:1; Rare:61 | ||||
chr9:122159708-122159921 | Rare:78 | ||||
chr9:125189771-125190029 | Common:1; Rare:91 | ||||
chr9:128275914-128276246 | Common:4; Rare:136 | ||||
chr9:128947583-128947714 | Common:1; Rare:54; Clinvar:2; Clinvar (benign):1 | ||||
chr9:129835237-129835449 | Common:2; Rare:84 | ||||
chr9:132878269-132878370 | Common:1; Rare:37 | ||||
chr9:133030467-133030742 | Common:4; Rare:71 | ||||
chr9:133348043-133348221 | Common:2; Rare:57 | ||||
chr9:133356402-133356552 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr9:137205633-137205735 | Rare:40 |