| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:15270118-15270258 | Rare:20 | ||||
| chrX:15335511-15335723 | Common:3; Rare:49; Clinvar (benign):1 | ||||
| chrX:16719463-16719690 | Rare:67 | ||||
| chrX:16786201-16786483 | Common:1; Rare:54 | ||||
| chrX:16870172-16870728 | Common:3; Rare:131 | ||||
| chrX:19670887-19670981 | Rare:20 | ||||
| chrX:23907716-23908004 | Rare:58 | ||||
| chrX:24149638-24149768 | Rare:25 | ||||
| chrX:30653140-30653425 | Common:2; Rare:76 | ||||
| chrX:38327471-38327682 | Rare:53 | ||||
| chrX:40735810-40736024 | Common:1; Rare:41 | ||||
| chrX:41333832-41334185 | Common:3; Rare:89 | ||||
| chrX:45200778-45201046 | Common:2; Rare:49 | ||||
| chrX:46545377-46545556 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chrX:47144617-47144816 | Common:1; Rare:34 |