| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:37847498-37847666 | Rare:40 | ||||
| chrX:38220835-38220967 | Rare:24 | ||||
| chrX:38327407-38327742 | Common:1; Rare:82 | ||||
| chrX:38561284-38561555 | Common:3; Rare:71; Clinvar (benign):1 | ||||
| chrX:38801272-38801470 | Common:1; Rare:32 | ||||
| chrX:40580730-40581067 | Common:5; Rare:78; Clinvar (benign):3 | ||||
| chrX:40735786-40735930 | Common:1; Rare:35 | ||||
| chrX:41085202-41085498 | Common:3; Rare:85 | ||||
| chrX:41333176-41333948 | Common:4; Rare:170 | ||||
| chrX:41333982-41334283 | Common:4; Rare:79 | ||||
| chrX:41334551-41334675 | Rare:58 | ||||
| chrX:41334985-41335140 | Common:1; Rare:19 | ||||
| chrX:43882417-43882541 | Rare:41 | ||||
| chrX:44542796-44543090 | Common:1; Rare:62 | ||||
| chrX:46447180-46447338 | Rare:28 |