| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:103376391-103376933 | Common:1; Rare:75 | ||||
| chrX:103585455-103585682 | Common:3; Rare:46 | ||||
| chrX:103607796-103608073 | Rare:49 | ||||
| chrX:103628898-103629019 | Rare:16 | ||||
| chrX:103629425-103629545 | Common:1; Rare:34 | ||||
| chrX:104156882-104157069 | Common:1; Rare:29 | ||||
| chrX:107628269-107628528 | Common:1; Rare:35; Clinvar (benign):1 | ||||
| chrX:107716167-107716361 | Rare:35 | ||||
| chrX:107716363-107716900 | Common:1; Rare:91 | ||||
| chrX:107716928-107717088 | Common:2; Rare:16 | ||||
| chrX:107775600-107775622 | Rare:1 | ||||
| chrX:107775647-107775883 | Rare:46 | ||||
| chrX:107775907-107775983 | Common:1; Rare:11 | ||||
| chrX:108091513-108091822 | Rare:81 | ||||
| chrX:108438200-108438518 | Rare:56 |