| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:119574382-119574645 | Rare:53 | ||||
| chrX:119605801-119605937 | Rare:17 | ||||
| chrX:119693095-119693260 | Common:1; Rare:45 | ||||
| chrX:119791590-119791978 | Common:2; Rare:102 | ||||
| chrX:119852921-119853276 | Common:3; Rare:58; Clinvar (benign):3 | ||||
| chrX:119871621-119871914 | Common:2; Rare:61; Clinvar (benign):3 | ||||
| chrX:120560726-120560863 | Rare:22 | ||||
| chrX:120560917-120561119 | Rare:43 | ||||
| chrX:120603806-120604150 | Rare:64 | ||||
| chrX:120604580-120604776 | Rare:22 | ||||
| chrX:120629938-120630266 | Common:4; Rare:64 | ||||
| chrX:123184120-123184574 | Common:4; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
| chrX:123733005-123733095 | Rare:17; Clinvar (benign):1 | ||||
| chrX:123859669-123860042 | Common:2; Rare:55 | ||||
| chrX:123860116-123860194 | Rare:15 |