| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:123859669-123860283 | Common:2; Rare:103 | ||||
| chrX:123960350-123960752 | Rare:31 | ||||
| chrX:123961282-123961433 | Common:2; Rare:21 | ||||
| chrX:123961519-123961845 | Rare:45 | ||||
| chrX:129843808-129844075 | Rare:34 | ||||
| chrX:129906073-129906201 | Rare:31 | ||||
| chrX:130165647-130165937 | Rare:57; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130171850-130172088 | Common:2; Rare:64 | ||||
| chrX:130401873-130402035 | Common:2; Rare:49 | ||||
| chrX:132217959-132218282 | Rare:37 | ||||
| chrX:134373135-134373522 | Common:4; Rare:80; Clinvar (benign):1 | ||||
| chrX:135032181-135032380 | Rare:46 | ||||
| chrX:135032568-135032849 | Rare:48 | ||||
| chrX:135052090-135052263 | Common:1; Rare:55 | ||||
| chrX:135344672-135344824 | Rare:33 |