Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:110087610-110087908 | Rare:38 | ||||
chrX:111685250-111685367 | Common:1; Rare:18 | ||||
chrX:111698638-111698832 | Common:1; Rare:25 | ||||
chrX:111709302-111709549 | Rare:34 | ||||
chrX:115562697-115562711 | |||||
chrX:115600971-115601246 | Rare:39 | ||||
chrX:118431652-118431881 | Rare:34 | ||||
chrX:118606131-118606274 | Common:1; Rare:13 | ||||
chrX:119581371-119581596 | Rare:23 | ||||
chrX:119583085-119583135 | Rare:9 | ||||
chrX:119786359-119786516 | Common:1; Rare:18 | ||||
chrX:119851525-119851787 | Common:5; Rare:39; Clinvar (benign):1 | ||||
chrX:119931972-119932183 | Common:1; Rare:33 | ||||
chrX:123606311-123606509 | Rare:33 | ||||
chrX:123615912-123616205 | Rare:35 |