| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:41688937-41689059 | Common:1; Rare:11 | ||||
| chrX:46447162-46447318 | Rare:30 | ||||
| chrX:46545374-46545531 | Common:1; Rare:31; Clinvar (benign):1 | ||||
| chrX:47232917-47233026 | Rare:28 | ||||
| chrX:47483146-47483277 | Common:3; Rare:17 | ||||
| chrX:47560916-47561216 | Common:1; Rare:55 | ||||
| chrX:47659101-47659437 | Common:2; Rare:92 | ||||
| chrX:47836791-47836956 | Common:1; Rare:38 | ||||
| chrX:48003929-48004289 | Common:3; Rare:89 | ||||
| chrX:48508838-48509029 | Common:1; Rare:39 | ||||
| chrX:48573933-48573997 | Rare:11 | ||||
| chrX:48574204-48574558 | Common:2; Rare:97 | ||||
| chrX:48918980-48919297 | Rare:59 | ||||
| chrX:48958367-48958406 | Rare:7 | ||||
| chrX:49073980-49074148 | Rare:45 |