| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:48911607-48911703 | Rare:21; Clinvar (benign):4 | ||||
| chrX:48958363-48958581 | Rare:46 | ||||
| chrX:49002127-49002573 | Common:2; Rare:80 | ||||
| chrX:49073983-49074173 | Rare:47 | ||||
| chrX:49079854-49079953 | Rare:15 | ||||
| chrX:49171590-49171957 | Common:3; Rare:46 | ||||
| chrX:49200149-49200363 | Rare:58; Clinvar:1 | ||||
| chrX:50470823-50471069 | Rare:36 | ||||
| chrX:51332465-51332865 | Common:2; Rare:151 | ||||
| chrX:51496535-51496882 | Common:2; Rare:85 | ||||
| chrX:51743304-51743470 | Rare:25 | ||||
| chrX:51802964-51803094 | Rare:29 | ||||
| chrX:51893339-51893717 | Common:2; Rare:72 | ||||
| chrX:53225175-53225504 | Common:2; Rare:106 | ||||
| chrX:53422622-53422935 | Common:1; Rare:79 |