| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:153971181-153971285 | Rare:25 | ||||
| chrX:154354429-154354679 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):7 | ||||
| chrX:154374575-154374823 | Common:1; Rare:47 | ||||
| chrX:154398206-154398535 | Common:3; Rare:123 | ||||
| chrX:154409251-154409427 | Rare:30 | ||||
| chrX:154428467-154428689 | Common:2; Rare:39 | ||||
| chrX:154486578-154486906 | Common:1; Rare:62 | ||||
| chrX:154516144-154516504 | Common:4; Rare:74 | ||||
| chrX:154547553-154547639 | Common:1; Rare:23; Clinvar (benign):1 | ||||
| chrX:155026708-155027055 | Common:1; Rare:91 | ||||
| chrY:2935290-2935389 | |||||
| chrY:12905665-12905731 | |||||
| chrY:13479687-13479996 | Rare:1 | ||||
| chrY:19744700-19744983 | Rare:4 |