Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:34112094-34112423 | Rare:105 | ||||
chr20:34303266-34303387 | Common:1; Rare:68; Clinvar:3; Clinvar (benign):1 | ||||
chr20:34516278-34516451 | Common:3; Rare:69 | ||||
chr20:34677078-34677314 | Rare:61 | ||||
chr20:35147273-35147411 | Common:1; Rare:49 | ||||
chr20:35284545-35284880 | Common:2; Rare:90 | ||||
chr20:35411959-35412125 | Rare:59 | ||||
chr20:35455060-35455310 | Common:1; Rare:88 | ||||
chr20:35542353-35542544 | Rare:66 | ||||
chr20:35631490-35631731 | Common:3; Rare:83 | ||||
chr20:35664855-35665005 | Common:1; Rare:42 | ||||
chr20:35699143-35699274 | Rare:25 | ||||
chr20:35699298-35699587 | Rare:84; Clinvar (benign):3 | ||||
chr20:35742097-35742649 | Common:5; Rare:176 | ||||
chr20:36236440-36236503 | Rare:14 |