| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:48676353-48676615 | Common:1; Rare:57 | ||||
| chrX:48696584-48696781 | Rare:47 | ||||
| chrX:48898066-48898270 | Common:2; Rare:29 | ||||
| chrX:48911584-48911706 | Common:1; Rare:27; Clinvar (benign):6 | ||||
| chrX:48918987-48919291 | Rare:57 | ||||
| chrX:48958297-48958675 | Rare:81 | ||||
| chrX:48971814-48972154 | Rare:47 | ||||
| chrX:49002189-49002529 | Common:2; Rare:60 | ||||
| chrX:49043501-49043821 | Rare:56 | ||||
| chrX:49079771-49079942 | Rare:23 | ||||
| chrX:49186264-49186466 | Common:1; Rare:37 | ||||
| chrX:49200176-49200348 | Rare:46; Clinvar:1 | ||||
| chrX:49879389-49879630 | Rare:44 | ||||
| chrX:51802972-51803112 | Rare:31 | ||||
| chrX:51893334-51893754 | Common:2; Rare:80 |