Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:39170290-39170471 | Common:2; Rare:59 | ||||
chr14:39175002-39175279 | Common:3; Rare:96 | ||||
chr14:39267110-39267417 | Common:1; Rare:106 | ||||
chr14:44961859-44962239 | Common:3; Rare:117 | ||||
chr14:45253051-45253293 | Rare:65 | ||||
chr14:49598635-49599018 | Common:3; Rare:148 | ||||
chr14:49620596-49620786 | Common:2; Rare:62 | ||||
chr14:49892898-49893115 | Rare:90 | ||||
chr14:50312222-50312376 | Rare:56 | ||||
chr14:50944301-50944595 | Common:5; Rare:107; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:52314039-52314344 | Common:2; Rare:79 | ||||
chr14:52552444-52552890 | Common:1; Rare:137 | ||||
chr14:52695529-52695823 | Common:1; Rare:81 | ||||
chr14:52707055-52707216 | Common:1; Rare:73 | ||||
chr14:54488930-54489119 | Common:1; Rare:63 |