Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:15675624-15675751 | Common:1; Rare:31 | ||||
chrX:45771234-45771470 | Rare:25 | ||||
chrX:110087536-110087868 | Rare:37 | ||||
chrX:134549642-134549765 | Common:1; Rare:33 | ||||
chrX:135032935-135032982 | Rare:4 | ||||
chrX:154366134-154366369 | Common:3; Rare:70; Clinvar:7; Clinvar (benign):9 |