| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154428473-154428728 | Common:2; Rare:47 | ||||
| chrX:154465861-154465991 | Rare:29 | ||||
| chrX:154486559-154486776 | Rare:34 | ||||
| chrX:154490614-154490791 | Common:2; Rare:45 | ||||
| chrX:154516012-154516060 | Rare:8 | ||||
| chrX:154516140-154516501 | Common:4; Rare:74 | ||||
| chrX:154546801-154547001 | Rare:73 | ||||
| chrX:154547553-154547697 | Common:1; Rare:36; Clinvar (benign):1 | ||||
| chrX:154762589-154762949 | Common:4; Rare:84; Clinvar:2 | ||||
| chrX:155026999-155027068 | Rare:23 | ||||
| chrX:155071078-155071538 | Common:1; Rare:101 | ||||
| chrX:155612853-155613014 | Common:1; Rare:29 | ||||
| chrY:2935262-2935396 | |||||
| chrY:13479669-13480047 | Rare:1 | ||||
| chrY:19744532-19744983 | Rare:10 |