| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:47482579-47482665 | Common:5; Rare:19; Clinvar:2 | ||||
| chrX:47483159-47483241 | Common:1; Rare:13 | ||||
| chrX:47560916-47561227 | Common:1; Rare:57 | ||||
| chrX:47582194-47582508 | Rare:53 | ||||
| chrX:47650506-47650762 | Common:3; Rare:81 | ||||
| chrX:47659107-47659282 | Rare:48 | ||||
| chrX:47836781-47836953 | Common:1; Rare:38 | ||||
| chrX:48003969-48004273 | Common:2; Rare:76 | ||||
| chrX:48468294-48468424 | Common:1; Rare:16 | ||||
| chrX:48475874-48476287 | Rare:73 | ||||
| chrX:48508861-48509040 | Rare:35 | ||||
| chrX:48574425-48574545 | Rare:50 | ||||
| chrX:48574853-48574999 | Rare:42 | ||||
| chrX:48696364-48696777 | Common:3; Rare:91 | ||||
| chrX:48911622-48911715 | Rare:25; Clinvar (benign):4 |