Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:125204288-125204515 | Rare:25 | ||||
chrX:132382232-132382350 | Rare:28 | ||||
chrX:134549639-134549770 | Common:1; Rare:36 | ||||
chrX:135021653-135021926 | Common:2; Rare:75 | ||||
chrX:135021930-135021952 | Rare:9 | ||||
chrX:149940027-149940138 | Common:1; Rare:21 | ||||
chrX:153506834-153507180 | Common:2; Rare:87 | ||||
chrX:153766402-153766607 | Rare:35 | ||||
chrX:154362417-154362735 | Common:3; Rare:84; Clinvar:10; Clinvar (benign):11 | ||||
chrX:154366022-154366595 | Common:3; Rare:177; Clinvar:15; Clinvar (benign):20; Clinvar (pathogenic):1 | ||||
chrX:154368895-154369130 | Rare:43 | ||||
chrY:3002741-3002990 | Rare:1 |