| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:101052081-101052171 | Rare:8 | ||||
| chrX:101097894-101098225 | Common:1; Rare:61 | ||||
| chrX:101348680-101348827 | Common:3; Rare:27 | ||||
| chrX:101386141-101386399 | Rare:31 | ||||
| chrX:101390888-101391046 | Rare:55 | ||||
| chrX:101407845-101408282 | Common:5; Rare:82; Clinvar:2; Clinvar (benign):11 | ||||
| chrX:101617898-101618052 | Common:1; Rare:31 | ||||
| chrX:103310938-103311097 | Common:2; Rare:26 | ||||
| chrX:103686677-103687324 | Common:5; Rare:101 | ||||
| chrX:103919027-103919194 | Common:4; Rare:32 | ||||
| chrX:104112378-104112566 | Rare:43 | ||||
| chrX:104156906-104157052 | Common:1; Rare:25 | ||||
| chrX:107628290-107628517 | Common:1; Rare:30; Clinvar (benign):1 | ||||
| chrX:107717060-107717193 | Rare:18 | ||||
| chrX:108091521-108091818 | Rare:79 |