Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:123960651-123960869 | Rare:27 | ||||
chrX:123961540-123961825 | Rare:41 | ||||
chrX:130165687-130165962 | Rare:59; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chrX:130401895-130402015 | Common:2; Rare:36 | ||||
chrX:134796301-134796411 | Common:1; Rare:5 | ||||
chrX:135344625-135344823 | Common:1; Rare:38 | ||||
chrX:135973753-135973802 | Rare:17 | ||||
chrX:149540814-149541021 | Common:3; Rare:37 | ||||
chrX:149938414-149938648 | Common:2; Rare:60 | ||||
chrX:152830718-152831112 | Common:2; Rare:69 | ||||
chrX:153599108-153599433 | Common:15; Rare:69 | ||||
chrX:153724083-153724151 | Rare:12 | ||||
chrX:153724548-153724878 | Common:1; Rare:67 | ||||
chrX:153794324-153794667 | Common:1; Rare:109; Clinvar (benign):2 | ||||
chrX:153864463-153864589 | Rare:30; Clinvar:1 |