Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:136724896-136724935 | Common:1; Rare:6 | ||||
chr9:136847847-136848034 | Rare:50 | ||||
chrM:15816-16153 | |||||
chrX:284737-285004 | Common:1; Rare:69 | ||||
chrX:309091-309237 | Common:2; Rare:31 | ||||
chrX:315242-315529 | Common:7; Rare:99 | ||||
chrX:315664-315994 | |||||
chrX:2609154-2609425 | Rare:87 | ||||
chrX:15675619-15675725 | Rare:21 | ||||
chrX:18898854-18899139 | Rare:48 | ||||
chrX:33726051-33726388 | Rare:43 | ||||
chrX:53093872-53094219 | Rare:63 | ||||
chrX:55908044-55908247 | Rare:36 | ||||
chrX:65598746-65598792 | Common:1; Rare:5 | ||||
chrX:67545593-67545701 | Rare:27; Clinvar (pathogenic):1 |