| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:24647205-24647475 | Common:1; Rare:35 | ||||
| chrX:24693538-24693977 | Common:2; Rare:79 | ||||
| chrX:32155420-32155569 | Common:1; Rare:20; Clinvar:1 | ||||
| chrX:37847510-37847665 | Rare:39 | ||||
| chrX:38561278-38561625 | Common:3; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chrX:40580742-40581051 | Common:5; Rare:74; Clinvar (benign):3 | ||||
| chrX:41085569-41085883 | Rare:70 | ||||
| chrX:41333174-41333342 | Rare:41 | ||||
| chrX:41334522-41334610 | Rare:34 | ||||
| chrX:43973387-43973504 | Rare:14 | ||||
| chrX:44542796-44543080 | Common:1; Rare:61 | ||||
| chrX:46545377-46545534 | Common:1; Rare:30; Clinvar (benign):1 | ||||
| chrX:47144474-47144837 | Common:2; Rare:79; Clinvar (benign):1 | ||||
| chrX:47145005-47145302 | Rare:39 | ||||
| chrX:47218622-47218746 | Rare:62 |