| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:49101095-49101408 | Common:2; Rare:65 | ||||
| chrX:49123723-49123920 | Rare:40 | ||||
| chrX:49186283-49186335 | Rare:7 | ||||
| chrX:49186339-49186466 | Common:1; Rare:23 | ||||
| chrX:53082092-53082379 | Common:1; Rare:67 | ||||
| chrX:53422170-53422286 | Rare:31 | ||||
| chrX:53422596-53422765 | Common:1; Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
| chrX:54043891-54044044 | Rare:31 | ||||
| chrX:54357832-54358207 | Common:1; Rare:67 | ||||
| chrX:54440244-54440433 | Rare:29 | ||||
| chrX:54530046-54530338 | Common:2; Rare:41 | ||||
| chrX:55000185-55000442 | Common:1; Rare:56 | ||||
| chrX:55030940-55031383 | Common:1; Rare:56; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:55161097-55161276 | Rare:54 | ||||
| chrX:56729458-56729525 | Common:1; Rare:8 |