| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:48898195-48898259 | Common:1; Rare:10 | ||||
| chrX:48911622-48911703 | Rare:19; Clinvar (benign):4 | ||||
| chrX:48958320-48958671 | Rare:73 | ||||
| chrX:49002152-49002553 | Common:2; Rare:71 | ||||
| chrX:49073995-49074212 | Rare:51 | ||||
| chrX:49079854-49079963 | Rare:17 | ||||
| chrX:49171745-49171997 | Common:3; Rare:32 | ||||
| chrX:49200134-49200363 | Rare:61; Clinvar:1 | ||||
| chrX:50067491-50067623 | Rare:19; Clinvar:1; Clinvar (benign):2 | ||||
| chrX:51496530-51496971 | Common:2; Rare:108 | ||||
| chrX:51743327-51743474 | Rare:21 | ||||
| chrX:51893341-51893741 | Common:2; Rare:76 | ||||
| chrX:53422613-53422976 | Common:2; Rare:88; Clinvar (benign):1 | ||||
| chrX:53434341-53434498 | Common:1; Rare:38 | ||||
| chrX:53536225-53536502 | Common:3; Rare:52; Clinvar (benign):1 |