| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:119468209-119468552 | Common:3; Rare:108 | ||||
| chrX:119574400-119574594 | Rare:42 | ||||
| chrX:119791553-119791994 | Common:2; Rare:115 | ||||
| chrX:119852932-119853276 | Common:3; Rare:56; Clinvar (benign):3 | ||||
| chrX:119871621-119871909 | Common:2; Rare:61; Clinvar (benign):3 | ||||
| chrX:119943567-119943851 | Rare:55 | ||||
| chrX:120250767-120250905 | Common:3; Rare:26 | ||||
| chrX:120559857-120560247 | Rare:60 | ||||
| chrX:120560468-120560845 | Rare:58; Clinvar:2 | ||||
| chrX:120561376-120561715 | Common:1; Rare:54 | ||||
| chrX:120603797-120604154 | Rare:68 | ||||
| chrX:120604606-120604802 | Rare:25 | ||||
| chrX:123732963-123733097 | Rare:26; Clinvar (benign):1 | ||||
| chrX:123859714-123860061 | Common:2; Rare:51 | ||||
| chrX:123960321-123960552 | Rare:19 |