| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:46545377-46545556 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chrX:46836717-46837085 | Rare:67; Clinvar:3; Clinvar (benign):1 | ||||
| chrX:46912241-46912328 | Rare:17 | ||||
| chrX:47078319-47078484 | Common:2; Rare:26 | ||||
| chrX:47144659-47144837 | Common:1; Rare:28 | ||||
| chrX:47145089-47145358 | Rare:42 | ||||
| chrX:47191282-47191454 | Rare:18 | ||||
| chrX:47217767-47218414 | Common:2; Rare:101 | ||||
| chrX:47218678-47218723 | Rare:21 | ||||
| chrX:47232920-47233148 | Rare:74 | ||||
| chrX:47233306-47233525 | Rare:36 | ||||
| chrX:47482544-47482665 | Common:5; Rare:27; Clinvar:2 | ||||
| chrX:47482916-47483054 | Rare:27 | ||||
| chrX:47483163-47483277 | Common:3; Rare:15 | ||||
| chrX:47560951-47561227 | Common:1; Rare:50 |