| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:103832124-103832280 | Common:1; Rare:26 | ||||
| chrX:103918752-103918908 | Common:1; Rare:24 | ||||
| chrX:103919005-103919155 | Common:4; Rare:28 | ||||
| chrX:104112379-104112678 | Rare:65 | ||||
| chrX:104156896-104157070 | Common:1; Rare:29 | ||||
| chrX:107118571-107118899 | Common:3; Rare:61 | ||||
| chrX:107206419-107206665 | Rare:41 | ||||
| chrX:107628205-107628588 | Common:1; Rare:58; Clinvar (benign):1 | ||||
| chrX:107716404-107716838 | Common:1; Rare:72 | ||||
| chrX:108091506-108091841 | Rare:89 | ||||
| chrX:108439479-108439878 | Common:2; Rare:90 | ||||
| chrX:109537089-109537249 | Rare:35 | ||||
| chrX:109733150-109733403 | Common:1; Rare:56 | ||||
| chrX:110944120-110944611 | Rare:66 | ||||
| chrX:111096011-111096411 | Common:1; Rare:55 |