Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:119606407-119606548 | Rare:29 | ||||
chrX:123514484-123514521 | Rare:5 | ||||
chrX:123514528-123514587 | Rare:6 | ||||
chrX:124729674-124729701 | Rare:3 | ||||
chrX:134549639-134549783 | Common:1; Rare:38 | ||||
chrX:140783784-140784207 | Rare:91 | ||||
chrX:154366126-154366369 | Common:3; Rare:71; Clinvar:8; Clinvar (benign):9 | ||||
chrY:3002650-3002942 | Rare:1 | ||||
chrY:12421554-12421726 | Common:1; Rare:1 | ||||
chrY:19075996-19076159 | Rare:2 |