| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:120560910-120561145 | Rare:48 | ||||
| chrX:120561411-120561636 | Common:1; Rare:36 | ||||
| chrX:120604061-120604154 | Rare:23 | ||||
| chrX:120629922-120630259 | Common:4; Rare:65 | ||||
| chrX:123961281-123961433 | Common:2; Rare:21 | ||||
| chrX:123961540-123961843 | Rare:43 | ||||
| chrX:129779817-129779990 | Rare:25 | ||||
| chrX:129905981-129906201 | Rare:60 | ||||
| chrX:130110474-130110631 | Rare:38 | ||||
| chrX:130165744-130165918 | Rare:30; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:132023172-132023305 | Rare:33 | ||||
| chrX:132217724-132218012 | Common:1; Rare:38 | ||||
| chrX:135052100-135052363 | Common:2; Rare:72 | ||||
| chrX:135343990-135344221 | Common:1; Rare:37 | ||||
| chrX:135344626-135344835 | Common:1; Rare:40 |