| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:109536952-109537263 | Common:4; Rare:82 | ||||
| chrX:109659382-109659782 | Rare:102; Clinvar:1; Clinvar (benign):2 | ||||
| chrX:109733185-109733566 | Common:1; Rare:86 | ||||
| chrX:110002303-110002462 | Rare:25 | ||||
| chrX:110002886-110003154 | Common:2; Rare:51 | ||||
| chrX:110316857-110317786 | Rare:202; Clinvar (pathogenic):2 | ||||
| chrX:110318051-110318404 | Rare:97 | ||||
| chrX:110795815-110796026 | Rare:36 | ||||
| chrX:110943909-110944309 | Common:2; Rare:82 | ||||
| chrX:110944405-110944611 | Rare:28 | ||||
| chrX:111095959-111096217 | Rare:41 | ||||
| chrX:111410431-111410949 | Common:4; Rare:102; Clinvar (pathogenic):2 | ||||
| chrX:111412160-111412470 | Common:1; Rare:38 | ||||
| chrX:111680983-111681291 | Rare:78; Clinvar (benign):7 | ||||
| chrX:111681505-111681701 | Rare:74 |