| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:40735814-40736052 | Common:1; Rare:43 | ||||
| chrX:41333857-41334264 | Common:6; Rare:109 | ||||
| chrX:44542815-44543034 | Common:1; Rare:40 | ||||
| chrX:46545377-46545564 | Common:1; Rare:44; Clinvar (benign):1 | ||||
| chrX:47144661-47144813 | Rare:25 | ||||
| chrX:47144912-47145297 | Rare:51 | ||||
| chrX:47202493-47202785 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
| chrX:47483169-47483242 | Common:1; Rare:10 | ||||
| chrX:48475874-48476354 | Rare:79 | ||||
| chrX:48574389-48574581 | Common:1; Rare:68 | ||||
| chrX:48574869-48574986 | Rare:34 | ||||
| chrX:48597666-48597877 | Common:1; Rare:24 | ||||
| chrX:49079800-49080054 | Rare:37 | ||||
| chrX:50643612-50643985 | Rare:51 | ||||
| chrX:53422596-53422918 | Common:2; Rare:90; Clinvar:1; Clinvar (benign):1 |