Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:133356436-133356607 | Common:1; Rare:79; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr9:133376015-133376366 | Common:1; Rare:126 | ||||
chr9:137188552-137188702 | Common:2; Rare:69 | ||||
chr9:137618846-137619029 | Common:1; Rare:73 | ||||
chrM:2468-3075 | |||||
chrX:13734546-13734751 | Common:2; Rare:52 | ||||
chrX:19670905-19670981 | Rare:17 | ||||
chrX:23907842-23908068 | Rare:43 | ||||
chrX:47144663-47144813 | Rare:25 | ||||
chrX:47145092-47145273 | Rare:28 | ||||
chrX:47232914-47233030 | Rare:30 | ||||
chrX:47582251-47582471 | Rare:33 | ||||
chrX:48911637-48911706 | Rare:14; Clinvar (benign):3 | ||||
chrX:53422645-53422920 | Common:1; Rare:64 | ||||
chrX:55000196-55000390 | Rare:38 |