| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154428467-154428707 | Common:2; Rare:43 | ||||
| chrX:154465775-154465985 | Common:2; Rare:50 | ||||
| chrX:154486574-154486760 | Rare:29 | ||||
| chrX:154516120-154516493 | Common:4; Rare:73 | ||||
| chrX:154547533-154547660 | Common:1; Rare:31; Clinvar (benign):1 | ||||
| chrX:155026912-155026919 | Rare:1 | ||||
| chrX:155026954-155027068 | Rare:32 | ||||
| chrX:155071051-155071520 | Common:1; Rare:100 | ||||
| chrX:155216253-155216480 | Rare:41 | ||||
| chrX:155881181-155881413 | Common:2; Rare:67 | ||||
| chrY:2935339-2935395 | |||||
| chrY:13479384-13479674 | Common:1; Rare:31 | ||||
| chrY:13479698-13480139 | |||||
| chrY:19744700-19744846 | Rare:3 | ||||
| chrY:19744905-19744983 | Rare:1 |