| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:153722367-153722474 | Rare:16 | ||||
| chrX:153871116-153871287 | Rare:37; Clinvar (benign):1 | ||||
| chrX:153878962-153879248 | Rare:39 | ||||
| chrX:153883390-153883487 | Common:1; Rare:17 | ||||
| chrX:154435458-154435704 | Rare:43 | ||||
| chrY:7273846-7273990 | |||||
| chrY:12662126-12662631 | Rare:6 | ||||
| chrY:13869107-13869178 | |||||
| chrY:19075964-19076172 | Rare:2 | ||||
| chrY:19566998-19567458 | Rare:12 |