| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:119871638-119872005 | Common:1; Rare:79; Clinvar (benign):3 | ||||
| chrX:119943620-119943838 | Rare:40 | ||||
| chrX:120250556-120250872 | Common:4; Rare:48 | ||||
| chrX:120560747-120560858 | Rare:14 | ||||
| chrX:120603838-120604164 | Rare:65 | ||||
| chrX:120629938-120630346 | Common:4; Rare:83 | ||||
| chrX:123733018-123733147 | Rare:21 | ||||
| chrX:123960350-123960705 | Rare:25 | ||||
| chrX:123961264-123961433 | Common:2; Rare:22 | ||||
| chrX:123961540-123961845 | Rare:43 | ||||
| chrX:129905945-129906205 | Rare:67 | ||||
| chrX:132023145-132023305 | Rare:41 | ||||
| chrX:132217719-132218012 | Common:1; Rare:39 | ||||
| chrX:132218044-132218278 | Rare:23 | ||||
| chrX:134915205-134915426 | Common:1; Rare:34 |