| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:103629431-103629565 | Common:1; Rare:33 | ||||
| chrX:103686648-103687028 | Common:4; Rare:53 | ||||
| chrX:103687060-103687351 | Common:1; Rare:51 | ||||
| chrX:103687989-103688207 | Common:1; Rare:33 | ||||
| chrX:103776630-103776875 | Common:2; Rare:26 | ||||
| chrX:103832185-103832454 | Common:2; Rare:46 | ||||
| chrX:103919027-103919194 | Common:4; Rare:32 | ||||
| chrX:104112386-104112586 | Rare:48 | ||||
| chrX:104156894-104157069 | Common:1; Rare:29 | ||||
| chrX:106168153-106168430 | Rare:44 | ||||
| chrX:106802439-106802792 | Common:1; Rare:62 | ||||
| chrX:107118775-107118899 | Common:2; Rare:27 | ||||
| chrX:107206392-107206668 | Common:1; Rare:47 | ||||
| chrX:107628235-107628541 | Common:1; Rare:43; Clinvar (benign):1 | ||||
| chrX:107716268-107716852 | Common:1; Rare:101 |