| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:47582001-47582488 | Common:1; Rare:71 | ||||
| chrX:47629814-47630064 | Common:1; Rare:33; Clinvar (benign):1 | ||||
| chrX:47630128-47630131 | |||||
| chrX:47659103-47659236 | Rare:40 | ||||
| chrX:48003969-48004283 | Common:3; Rare:76 | ||||
| chrX:48508848-48509029 | Common:1; Rare:38 | ||||
| chrX:48574241-48574558 | Common:2; Rare:93 | ||||
| chrX:48574810-48574999 | Rare:60 | ||||
| chrX:48575085-48575241 | Common:2; Rare:37 | ||||
| chrX:48683739-48683900 | Rare:30 | ||||
| chrX:48911636-48911725 | Rare:21; Clinvar (benign):3 | ||||
| chrX:48919016-48919297 | Rare:43 | ||||
| chrX:48958336-48958681 | Rare:69 | ||||
| chrX:49171734-49171985 | Common:3; Rare:31 | ||||
| chrX:49172029-49172107 | Rare:20 |