| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:9464020-9464500 | Rare:124 | ||||
| chrX:9501804-9501980 | Common:1; Rare:34 | ||||
| chrX:9691450-9692080 | Common:8; Rare:162 | ||||
| chrX:10578940-10579680 | Common:1; Rare:161 | ||||
| chrX:12956260-12956640 | Common:2; Rare:96 | ||||
| chrX:13827388-13827491 | Common:1; Rare:13 | ||||
| chrX:15674717-15675010 | Common:3; Rare:117 | ||||
| chrX:15675020-15675220 | Common:5; Rare:96 | ||||
| chrX:15675329-15675777 | Common:13; Rare:171 | ||||
| chrX:16771828-16772080 | Common:4; Rare:114 | ||||
| chrX:18674730-18675390 | Common:3; Rare:283 | ||||
| chrX:18702620-18703140 | Common:6; Rare:106 | ||||
| chrX:18886650-18887080 | Rare:93 | ||||
| chrX:19349514-19350089 | Common:4; Rare:124; Clinvar (benign):4 | ||||
| chrX:19673520-19673877 | Rare:75 |