| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:149540909-149541082 | Common:3; Rare:32 | ||||
| chrX:149938404-149938620 | Common:1; Rare:54 | ||||
| chrX:150831247-150831569 | Common:1; Rare:34 | ||||
| chrX:150898535-150898911 | Common:4; Rare:100 | ||||
| chrX:151397051-151397273 | Common:4; Rare:112 | ||||
| chrX:152830707-152831094 | Common:2; Rare:69 | ||||
| chrX:153599079-153599351 | Common:13; Rare:56 | ||||
| chrX:153724064-153724146 | Common:1; Rare:14 | ||||
| chrX:153724559-153724871 | Common:1; Rare:65 | ||||
| chrX:153786811-153787104 | Rare:68 | ||||
| chrX:153794056-153794186 | Common:1; Rare:19 | ||||
| chrX:153794258-153794736 | Common:1; Rare:147; Clinvar (benign):2 | ||||
| chrX:153971136-153971285 | Rare:34 | ||||
| chrX:153972412-153972790 | Common:2; Rare:116 | ||||
| chrX:154353083-154353330 | Common:3; Rare:57; Clinvar:3; Clinvar (benign):2 |