| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:11111129-11111484 | Common:4; Rare:65 | ||||
| chrX:11265727-11265966 | Rare:37 | ||||
| chrX:11427548-11427909 | Common:2; Rare:73 | ||||
| chrX:11759476-11759692 | Rare:27 | ||||
| chrX:13688969-13689235 | Common:2; Rare:73 | ||||
| chrX:13734530-13734870 | Common:3; Rare:101; Clinvar (benign):1 | ||||
| chrX:14873045-14873533 | Common:2; Rare:95 | ||||
| chrX:15270137-15270267 | Rare:16 | ||||
| chrX:15493177-15493415 | Common:1; Rare:46 | ||||
| chrX:15854142-15854373 | Common:3; Rare:44 | ||||
| chrX:15854699-15855029 | Rare:69 | ||||
| chrX:16719488-16719806 | Common:1; Rare:87 | ||||
| chrX:16786175-16786575 | Common:2; Rare:87 | ||||
| chrX:16870144-16870763 | Common:3; Rare:143 | ||||
| chrX:18425344-18425644 | Common:2; Rare:72; Clinvar:1; Clinvar (benign):3 |