| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:149938404-149938761 | Common:3; Rare:85 | ||||
| chrX:152830708-152831110 | Common:2; Rare:72 | ||||
| chrX:153599094-153599363 | Common:13; Rare:53 | ||||
| chrX:153724064-153724151 | Common:1; Rare:16 | ||||
| chrX:153794073-153794236 | Common:2; Rare:27 | ||||
| chrX:153794300-153794668 | Common:1; Rare:114; Clinvar (benign):2 | ||||
| chrX:153934943-153935339 | Common:1; Rare:91 | ||||
| chrX:153971183-153971271 | Rare:23 | ||||
| chrX:154019831-154020017 | Rare:37 | ||||
| chrX:154398826-154399029 | Common:2; Rare:44 | ||||
| chrX:154409209-154409442 | Rare:36 | ||||
| chrX:154428473-154428737 | Common:2; Rare:52; Clinvar:1 | ||||
| chrX:154486549-154486782 | Rare:36 | ||||
| chrX:154547550-154547661 | Common:1; Rare:29; Clinvar (benign):1 |