| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:139204996-139205197 | Rare:37 | ||||
| chrX:139205449-139205707 | Rare:37 | ||||
| chrX:139932971-139933281 | Rare:59 | ||||
| chrX:139933490-139933632 | Rare:21 | ||||
| chrX:140505058-140505348 | Common:2; Rare:61; Clinvar:1 | ||||
| chrX:140505864-140506177 | Rare:57 | ||||
| chrX:141177089-141177412 | Common:1; Rare:52 | ||||
| chrX:143636076-143636317 | Common:2; Rare:24 | ||||
| chrX:145817579-145817840 | Common:2; Rare:43 | ||||
| chrX:147911752-147912173 | Common:4; Rare:133 | ||||
| chrX:147912584-147912984 | Common:2; Rare:95 | ||||
| chrX:148500784-148501281 | Common:4; Rare:153; Clinvar (benign):3 | ||||
| chrX:149505288-149505468 | Rare:42 | ||||
| chrX:149540004-149540330 | Common:1; Rare:28 | ||||
| chrX:149540431-149540631 | Common:1; Rare:22 |