| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrM:15883-16042 | |||||
| chrX:1600519-1600609 | Rare:23 | ||||
| chrX:2609154-2609421 | Rare:85 | ||||
| chrX:15675083-15675104 | Rare:3 | ||||
| chrX:15675346-15675478 | Common:4; Rare:24 | ||||
| chrX:15675606-15675735 | Common:1; Rare:24 | ||||
| chrX:46576069-46576249 | Common:1; Rare:23 | ||||
| chrX:47091452-47091779 | Common:1; Rare:51 | ||||
| chrX:47235668-47235876 | Rare:16 | ||||
| chrX:53093901-53094205 | Rare:54 | ||||
| chrX:53094267-53094411 | Rare:27 | ||||
| chrX:55489832-55489853 | Rare:1 | ||||
| chrX:55908044-55908247 | Rare:36 | ||||
| chrX:67545524-67545701 | Rare:40; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:70962765-70963024 | Common:1; Rare:29 |