| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154428448-154428794 | Common:3; Rare:71; Clinvar:1 | ||||
| chrX:154443993-154444265 | Common:6; Rare:72 | ||||
| chrX:154486545-154486760 | Rare:29 | ||||
| chrX:154516114-154516537 | Common:4; Rare:83 | ||||
| chrX:154547522-154547639 | Common:1; Rare:30; Clinvar (benign):1 | ||||
| chrX:154762585-154762938 | Common:4; Rare:79; Clinvar:2 | ||||
| chrX:154805340-154805536 | Rare:41 | ||||
| chrX:155026680-155027069 | Common:1; Rare:100 | ||||
| chrX:155071101-155071554 | Common:1; Rare:107 | ||||
| chrX:155216270-155216534 | Rare:49 | ||||
| chrY:2841527-2841632 | Rare:9 | ||||
| chrY:2841838-2841951 | Rare:5 | ||||
| chrY:2935265-2935389 | |||||
| chrY:12904685-12904895 | Rare:4 | ||||
| chrY:13479948-13480114 |