| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:136169351-136169843 | Common:2; Rare:70 | ||||
| chrX:141177072-141177302 | Common:1; Rare:28 | ||||
| chrX:149540904-149541065 | Common:3; Rare:31 | ||||
| chrX:149938440-149938628 | Common:1; Rare:49 | ||||
| chrX:151396915-151397257 | Common:5; Rare:150 | ||||
| chrX:152830706-152831098 | Common:2; Rare:69 | ||||
| chrX:152941527-152941711 | Common:1; Rare:43 | ||||
| chrX:153599036-153599356 | Common:15; Rare:61 | ||||
| chrX:153724557-153724867 | Common:1; Rare:65 | ||||
| chrX:153786811-153787097 | Rare:66 | ||||
| chrX:153794313-153794742 | Common:1; Rare:133; Clinvar (benign):2 | ||||
| chrX:153944614-153944743 | Common:2; Rare:29 | ||||
| chrX:153971168-153971278 | Rare:25 | ||||
| chrX:154354436-154354634 | Rare:31; Clinvar (benign):2 | ||||
| chrX:154358311-154358446 | Common:2; Rare:24; Clinvar (benign):4 |