| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:20267061-20267282 | Common:1; Rare:40 | ||||
| chrX:23782984-23783329 | Common:5; Rare:73 | ||||
| chrX:23783332-23784014 | Common:4; Rare:171 | ||||
| chrX:23907724-23908070 | Rare:72 | ||||
| chrX:24054899-24054974 | Rare:21 | ||||
| chrX:30653124-30653436 | Common:2; Rare:81 | ||||
| chrX:40735814-40736088 | Common:1; Rare:51 | ||||
| chrX:41333971-41334283 | Common:4; Rare:81 | ||||
| chrX:41334533-41334634 | Rare:45 | ||||
| chrX:44542846-44543034 | Common:1; Rare:33 | ||||
| chrX:46545393-46545556 | Rare:36 | ||||
| chrX:47144668-47144837 | Common:1; Rare:27 | ||||
| chrX:47145089-47145352 | Rare:38 | ||||
| chrX:47202575-47202728 | Common:1; Rare:34; Clinvar (benign):1 | ||||
| chrX:47232903-47233036 | Rare:37 |