| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:24149576-24149790 | Rare:34 | ||||
| chrX:24465038-24465386 | Common:4; Rare:99 | ||||
| chrX:30653112-30653429 | Common:2; Rare:83 | ||||
| chrX:37349174-37349404 | Common:2; Rare:34 | ||||
| chrX:37847506-37847676 | Common:1; Rare:42 | ||||
| chrX:38220761-38221044 | Rare:73 | ||||
| chrX:38561401-38561564 | Common:3; Rare:41; Clinvar (benign):1 | ||||
| chrX:40097464-40097597 | Rare:18 | ||||
| chrX:40146577-40146655 | Rare:10 | ||||
| chrX:40580725-40581078 | Common:5; Rare:80; Clinvar (benign):3 | ||||
| chrX:40735300-40735709 | Rare:102 | ||||
| chrX:40735725-40735962 | Common:1; Rare:58 | ||||
| chrX:41333417-41333971 | Common:4; Rare:118 | ||||
| chrX:41334321-41334675 | Common:2; Rare:130 | ||||
| chrX:41334978-41335136 | Common:1; Rare:20 |