| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154516146-154516563 | Common:4; Rare:87 | ||||
| chrX:154547551-154547645 | Common:1; Rare:23; Clinvar (benign):1 | ||||
| chrX:155026673-155027069 | Common:1; Rare:100 | ||||
| chrX:155046900-155047068 | Rare:16 | ||||
| chrX:155071038-155071533 | Common:1; Rare:103 | ||||
| chrX:155881173-155881432 | Common:3; Rare:70 | ||||
| chrY:2935290-2935389 | |||||
| chrY:12905682-12905723 | |||||
| chrY:13479384-13479422 | |||||
| chrY:14524261-14524541 | Common:1; Rare:2 | ||||
| chrY:19744705-19744978 | Rare:3 |