Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:118135938-118136247 | Common:2; Rare:96 | ||||
chr12:118372846-118373188 | Common:2; Rare:92 | ||||
chr12:119178550-119178843 | Common:1; Rare:61; Clinvar:1 | ||||
chr12:119178882-119179122 | Common:1; Rare:39; Clinvar:2; Clinvar (benign):1 | ||||
chr12:119179127-119179688 | Rare:167; Clinvar:10; Clinvar (benign):4 | ||||
chr12:120116641-120116935 | Common:5; Rare:84 | ||||
chr12:120194697-120194791 | Rare:36 | ||||
chr12:120201081-120201354 | Common:2; Rare:88 | ||||
chr12:120446344-120446489 | Common:2; Rare:66 | ||||
chr12:120469446-120469906 | Common:6; Rare:150 | ||||
chr12:120495845-120496240 | Common:7; Rare:131 | ||||
chr12:120497964-120498222 | Rare:48 | ||||
chr12:120581342-120581577 | Common:1; Rare:80 | ||||
chr12:121210035-121210152 | Common:2; Rare:37 | ||||
chr12:121580241-121580477 | Rare:75 |