| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:120560468-120560858 | Rare:61; Clinvar:2 | ||||
| chrX:120560909-120561246 | Rare:72 | ||||
| chrX:120561395-120561715 | Common:1; Rare:51 | ||||
| chrX:120603797-120604156 | Rare:69 | ||||
| chrX:120629916-120630270 | Common:4; Rare:68 | ||||
| chrX:123733025-123733152 | Rare:20 | ||||
| chrX:123960350-123960748 | Rare:28 | ||||
| chrX:123961264-123961432 | Common:2; Rare:22 | ||||
| chrX:123961554-123961828 | Rare:40 | ||||
| chrX:129905975-129906195 | Rare:59 | ||||
| chrX:130165703-130165908 | Rare:40; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130339786-130339971 | Rare:28 | ||||
| chrX:130401874-130402029 | Common:2; Rare:48 | ||||
| chrX:132023135-132023345 | Rare:51 | ||||
| chrX:132217965-132218291 | Rare:40 |