Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:119236563-119236618 | Rare:14 | ||||
chrX:119468222-119468497 | Common:3; Rare:95 | ||||
chrX:119791596-119791720 | Rare:51 | ||||
chrX:119871683-119871914 | Common:1; Rare:56; Clinvar (benign):3 | ||||
chrX:123733017-123733152 | Rare:21 | ||||
chrX:130165699-130165908 | Rare:42; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chrX:135344635-135344812 | Common:1; Rare:31 | ||||
chrX:139205019-139205212 | Rare:42 | ||||
chrX:141177076-141177289 | Common:1; Rare:26 | ||||
chrX:149540913-149541012 | Common:2; Rare:16 | ||||
chrX:152830688-152831050 | Common:2; Rare:69 | ||||
chrX:153794330-153794690 | Common:1; Rare:112; Clinvar (benign):2 | ||||
chrX:153971178-153971326 | Rare:36 | ||||
chrX:154428457-154428689 | Common:2; Rare:40 | ||||
chrX:154516207-154516520 | Common:3; Rare:59 |