| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:153411279-153411525 | Common:2; Rare:65 | ||||
| chrX:153463063-153463281 | Rare:41 | ||||
| chrX:153925541-153925712 | Rare:39 | ||||
| chrX:154366028-154366369 | Common:3; Rare:103; Clinvar:13; Clinvar (benign):14 | ||||
| chrX:154366549-154366775 | Rare:52; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chrY:3002348-3002498 | Rare:2 | ||||
| chrY:3002518-3002539 | |||||
| chrY:3002741-3003009 | Rare:2 | ||||
| chrY:6911750-6911990 | Rare:1 | ||||
| chrY:12662193-12662520 | Rare:3 | ||||
| chrY:19075973-19076170 | Rare:2 | ||||
| chrY:19077126-19077191 |