| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:47145097-47145301 | Rare:31 | ||||
| chrX:47482568-47482665 | Common:5; Rare:22; Clinvar:2 | ||||
| chrX:47483177-47483285 | Common:3; Rare:14 | ||||
| chrX:47836610-47836949 | Common:1; Rare:73 | ||||
| chrX:48468302-48468361 | Rare:11 | ||||
| chrX:48508837-48509026 | Common:1; Rare:38 | ||||
| chrX:48574869-48575015 | Rare:42 | ||||
| chrX:48696583-48696777 | Rare:43 | ||||
| chrX:48958363-48958682 | Rare:55 | ||||
| chrX:49002196-49002553 | Common:2; Rare:63 | ||||
| chrX:49079831-49079988 | Rare:25 | ||||
| chrX:50643692-50643993 | Rare:37 | ||||
| chrX:53422613-53422827 | Common:1; Rare:61; Clinvar (benign):1 | ||||
| chrX:54530064-54530309 | Common:2; Rare:35 | ||||
| chrX:55161097-55161249 | Rare:46 |