| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:71365907-71366246 | Common:4; Rare:62 | ||||
| chrX:72238993-72239121 | Rare:33 | ||||
| chrX:74614574-74614893 | Common:1; Rare:73 | ||||
| chrX:75156268-75156369 | Common:2; Rare:26 | ||||
| chrX:75273989-75274238 | Rare:36 | ||||
| chrX:75523018-75523144 | Rare:28 | ||||
| chrX:75523244-75523535 | Common:2; Rare:39 | ||||
| chrX:76172769-76173086 | Rare:54 | ||||
| chrX:77895395-77895731 | Rare:96; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chrX:78103962-78104371 | Common:4; Rare:149 | ||||
| chrX:79367283-79367581 | Common:1; Rare:56 | ||||
| chrX:81201876-81202243 | Rare:62 | ||||
| chrX:100928610-100928829 | Rare:34 | ||||
| chrX:100928887-100929011 | Common:1; Rare:19 | ||||
| chrX:100929416-100929578 | Rare:18 |