Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:152698649-152698816 | Rare:2 | ||||
chrX:152733679-152733840 | Common:1; Rare:49 | ||||
chrX:152830718-152831094 | Common:2; Rare:65 | ||||
chrX:153794334-153794679 | Common:1; Rare:109; Clinvar (benign):2 | ||||
chrX:154428448-154428689 | Common:2; Rare:43 | ||||
chrX:154547541-154547639 | Common:1; Rare:25; Clinvar (benign):1 | ||||
chrX:155026991-155027050 | Rare:20 | ||||
chrX:155071106-155071520 | Common:1; Rare:87 |