| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:123960349-123960743 | Rare:28 | ||||
| chrX:123961264-123961432 | Common:2; Rare:22 | ||||
| chrX:123961560-123961819 | Rare:37 | ||||
| chrX:126552755-126553037 | Rare:55 | ||||
| chrX:129523182-129523716 | Common:4; Rare:123 | ||||
| chrX:129540485-129540774 | Rare:57; Clinvar:3; Clinvar (benign):1 | ||||
| chrX:129906039-129906197 | Rare:44 | ||||
| chrX:129982413-129982643 | Common:1; Rare:36 | ||||
| chrX:130165649-130165977 | Rare:73; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130339707-130340001 | Rare:51 | ||||
| chrX:130401873-130402035 | Common:2; Rare:49 | ||||
| chrX:130903159-130903323 | Rare:38 | ||||
| chrX:132023151-132023276 | Rare:34 | ||||
| chrX:132217734-132218291 | Common:1; Rare:70 | ||||
| chrX:132219427-132219513 | Rare:6 |