Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:35826717-35826926 | Common:1; Rare:55 | ||||
chr14:36320557-36320811 | Common:4; Rare:84 | ||||
chr14:37197843-37198087 | Common:3; Rare:80 | ||||
chr14:38256056-38256364 | Common:1; Rare:80 | ||||
chr14:39170203-39170483 | Common:3; Rare:75 | ||||
chr14:39175168-39175321 | Common:2; Rare:67 | ||||
chr14:39267067-39267472 | Common:2; Rare:148 | ||||
chr14:39431620-39431662 | Common:1; Rare:13 | ||||
chr14:39432401-39432660 | Common:6; Rare:88 | ||||
chr14:39432887-39433005 | Rare:41 | ||||
chr14:44961845-44962259 | Common:3; Rare:126 | ||||
chr14:45135723-45136010 | Common:1; Rare:64 | ||||
chr14:45253047-45253312 | Rare:72 | ||||
chr14:45253454-45253575 | Common:2; Rare:52 | ||||
chr14:49586298-49586776 | Common:1; Rare:246; Clinvar (benign):1 |