Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:135022468-135022755 | Rare:60 | ||||
chrX:135052100-135052263 | Common:1; Rare:49 | ||||
chrX:135344634-135344823 | Common:1; Rare:35 | ||||
chrX:135973695-135973872 | Rare:59 | ||||
chrX:139205015-139205161 | Rare:26 | ||||
chrX:139222835-139223090 | Rare:26 | ||||
chrX:141177065-141177314 | Common:1; Rare:32 | ||||
chrX:149540909-149541087 | Common:3; Rare:32 | ||||
chrX:149938440-149938632 | Common:1; Rare:50 | ||||
chrX:151397051-151397292 | Common:4; Rare:121 | ||||
chrX:151974674-151974991 | Common:1; Rare:83 | ||||
chrX:152830712-152831094 | Common:2; Rare:67 | ||||
chrX:152941520-152941701 | Common:1; Rare:44 | ||||
chrX:153724352-153724726 | Common:3; Rare:95 | ||||
chrX:153794307-153794690 | Common:1; Rare:116; Clinvar (benign):2 |