| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:47078389-47078453 | Rare:8 | ||||
| chrX:47144579-47144837 | Common:1; Rare:50 | ||||
| chrX:47145117-47145347 | Rare:36 | ||||
| chrX:47202933-47203132 | Rare:45; Clinvar (benign):2 | ||||
| chrX:47218672-47218775 | Rare:48 | ||||
| chrX:47233343-47233459 | Rare:20 | ||||
| chrX:47482533-47482665 | Common:5; Rare:29; Clinvar:2 | ||||
| chrX:47483151-47483277 | Common:3; Rare:17 | ||||
| chrX:47561000-47561237 | Common:1; Rare:43 | ||||
| chrX:47659107-47659275 | Rare:47 | ||||
| chrX:47836804-47836962 | Common:1; Rare:33 | ||||
| chrX:48003960-48004142 | Rare:49 | ||||
| chrX:48468294-48468491 | Common:1; Rare:25 | ||||
| chrX:48475947-48476263 | Rare:56 | ||||
| chrX:48508868-48509026 | Rare:28 |