Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:123961554-123961812 | Rare:38 | ||||
chrX:129739089-129739145 | Common:1; Rare:5 | ||||
chrX:130165703-130165961 | Rare:54; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chrX:132218044-132218238 | Rare:10 | ||||
chrX:135344578-135344818 | Common:2; Rare:41 | ||||
chrX:135973738-135973860 | Rare:42 | ||||
chrX:135985344-135985450 | Rare:29 | ||||
chrX:141177061-141177314 | Common:1; Rare:34 | ||||
chrX:151397030-151397241 | Common:5; Rare:104 | ||||
chrX:152830712-152831088 | Common:2; Rare:67 | ||||
chrX:153724537-153724856 | Common:1; Rare:63 | ||||
chrX:153794313-153794705 | Common:1; Rare:123; Clinvar (benign):2 | ||||
chrX:154398634-154398807 | Common:1; Rare:41 | ||||
chrX:154409190-154409453 | Rare:40 | ||||
chrX:154428463-154428697 | Common:2; Rare:40 |