| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:48801364-48801423 | Common:1; Rare:7 | ||||
| chrX:48801674-48802016 | Rare:66 | ||||
| chrX:48898074-48898287 | Common:2; Rare:30 | ||||
| chrX:48911634-48911715 | Rare:21; Clinvar (benign):3 | ||||
| chrX:48958320-48958690 | Rare:73 | ||||
| chrX:49002193-49002347 | Rare:39 | ||||
| chrX:49079796-49079953 | Rare:20 | ||||
| chrX:49101110-49101408 | Common:2; Rare:62 | ||||
| chrX:49186304-49186482 | Common:1; Rare:29 | ||||
| chrX:49200158-49200363 | Rare:56; Clinvar:1 | ||||
| chrX:49922354-49922748 | Common:1; Rare:81 | ||||
| chrX:50814094-50814458 | Rare:73 | ||||
| chrX:51496540-51496917 | Common:2; Rare:87 | ||||
| chrX:51743353-51743463 | Rare:14 | ||||
| chrX:51802970-51803097 | Rare:30 |