| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:15335511-15335818 | Common:3; Rare:63; Clinvar (benign):1 | ||||
| chrX:15790382-15790571 | Rare:45 | ||||
| chrX:16719366-16719697 | Rare:85 | ||||
| chrX:16786167-16786505 | Common:2; Rare:73 | ||||
| chrX:16870400-16870736 | Common:1; Rare:76 | ||||
| chrX:19343675-19343997 | Common:6; Rare:90 | ||||
| chrX:19670884-19670990 | Rare:22 | ||||
| chrX:20267057-20267369 | Common:2; Rare:52 | ||||
| chrX:21940489-21940864 | Common:2; Rare:93 | ||||
| chrX:23667280-23667663 | Common:3; Rare:111 | ||||
| chrX:23743189-23743481 | Common:7; Rare:53 | ||||
| chrX:23783022-23783269 | Common:4; Rare:52 | ||||
| chrX:23907705-23908068 | Common:1; Rare:76 | ||||
| chrX:24054891-24054987 | Rare:35 | ||||
| chrX:30653137-30653436 | Common:2; Rare:78 |