Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:46327637-46327772 | Common:1; Rare:17 | ||||
chrX:74292029-74292163 | Common:2; Rare:14 | ||||
chrX:102769083-102769161 | Common:1; Rare:8 | ||||
chrX:131830575-131830798 | Rare:34 | ||||
chrX:154362303-154362462 | Rare:45; Clinvar:3; Clinvar (benign):1 |