| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:120559867-120560262 | Rare:59 | ||||
| chrX:120560677-120561115 | Rare:79 | ||||
| chrX:120561345-120561698 | Common:1; Rare:59 | ||||
| chrX:120603740-120603985 | Rare:49 | ||||
| chrX:120603987-120604164 | Rare:32 | ||||
| chrX:120604278-120604573 | Rare:51 | ||||
| chrX:120604577-120604844 | Rare:33 | ||||
| chrX:120629905-120630352 | Common:5; Rare:87 | ||||
| chrX:123183831-123184418 | Common:2; Rare:95 | ||||
| chrX:123732993-123733105 | Rare:23; Clinvar (benign):1 | ||||
| chrX:123859634-123860061 | Common:2; Rare:61 | ||||
| chrX:123860068-123860208 | Rare:23 | ||||
| chrX:123960288-123960762 | Rare:42 | ||||
| chrX:123960765-123960881 | Rare:16 | ||||
| chrX:123961264-123961435 | Common:2; Rare:22 |