| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154546780-154546980 | Common:1; Rare:72 | ||||
| chrX:154547221-154547377 | Rare:28 | ||||
| chrX:154547553-154547660 | Common:1; Rare:26; Clinvar (benign):1 | ||||
| chrX:155022711-155022872 | Rare:16 | ||||
| chrX:155026790-155027096 | Rare:84 | ||||
| chrX:155071025-155071527 | Common:2; Rare:105 | ||||
| chrY:2935262-2935400 | |||||
| chrY:12905633-12905736 | Rare:1 | ||||
| chrY:14524391-14524680 | Common:1; Rare:11 | ||||
| chrY:19744700-19744983 | Rare:4 |