Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:53093901-53094194 | Rare:53 | ||||
chrX:53094271-53094416 | Rare:26 | ||||
chrX:73944228-73944366 | Rare:34 | ||||
chrX:74292581-74292745 | Rare:25 | ||||
chrX:74420556-74420933 | Common:2; Rare:98 | ||||
chrX:154361343-154361779 | Common:1; Rare:86; Clinvar:9; Clinvar (benign):15 | ||||
chrX:154366372-154366584 | Rare:69; Clinvar:1; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chrY:12662148-12662386 | Rare:1 |