| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154486556-154486754 | Rare:29 | ||||
| chrX:154490654-154490776 | Common:1; Rare:32 | ||||
| chrX:154516114-154516563 | Common:4; Rare:90 | ||||
| chrX:154547553-154547679 | Common:1; Rare:34; Clinvar (benign):1 | ||||
| chrX:154762589-154762927 | Common:4; Rare:76; Clinvar:2 | ||||
| chrX:155026776-155027096 | Rare:88 | ||||
| chrX:155071051-155071520 | Common:1; Rare:100 |