| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:43743935-43744129 | Common:1; Rare:35; Clinvar:1 | ||||
| chrX:44873468-44873698 | Rare:62; Clinvar (benign):2 | ||||
| chrX:46545377-46545524 | Common:1; Rare:26; Clinvar (benign):1 | ||||
| chrX:47144647-47144756 | Rare:22 | ||||
| chrX:47145093-47145353 | Rare:39 | ||||
| chrX:47218659-47218737 | Rare:42 | ||||
| chrX:47482567-47482665 | Common:5; Rare:22; Clinvar:2 | ||||
| chrX:47483169-47483277 | Common:3; Rare:14 | ||||
| chrX:47561021-47561216 | Common:1; Rare:37 | ||||
| chrX:47561352-47561638 | Rare:48 | ||||
| chrX:47659086-47659275 | Rare:52 | ||||
| chrX:47836791-47836976 | Common:1; Rare:42 | ||||
| chrX:48071563-48071693 | Common:1; Rare:23 | ||||
| chrX:48475897-48476239 | Rare:57 | ||||
| chrX:48508861-48509027 | Rare:32 |