| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:155216270-155216507 | Rare:75 | ||||
| chrX:155612879-155613021 | Common:1; Rare:28 | ||||
| chrY:2787318-2788150 | Common:4; Rare:55; Clinvar (pathogenic):3 | ||||
| chrY:2841463-2841707 | Rare:19 | ||||
| chrY:2935068-2935445 | Common:1; Rare:2 | ||||
| chrY:6910240-6910722 | Rare:4 | ||||
| chrY:12904619-12904914 | Rare:19 | ||||
| chrY:14524486-14524687 | Common:1; Rare:11 | ||||
| chrY:19744703-19744961 | Rare:3 |