| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:107118759-107118907 | Common:2; Rare:32 | ||||
| chrX:107206281-107206672 | Common:2; Rare:76 | ||||
| chrX:107628290-107628528 | Common:1; Rare:31; Clinvar (benign):1 | ||||
| chrX:107716279-107716623 | Common:1; Rare:47 | ||||
| chrX:107775710-107775883 | Rare:35 | ||||
| chrX:107777320-107777490 | Common:2; Rare:17 | ||||
| chrX:108064619-108064717 | Rare:16 | ||||
| chrX:108091130-108091216 | Rare:12 | ||||
| chrX:108091492-108091829 | Rare:94 | ||||
| chrX:108439499-108440023 | Common:3; Rare:110 | ||||
| chrX:109537065-109537219 | Common:1; Rare:34 | ||||
| chrX:109733130-109733502 | Common:1; Rare:87 | ||||
| chrX:110317931-110318267 | Rare:88 | ||||
| chrX:111681106-111681302 | Rare:55; Clinvar (benign):7 | ||||
| chrX:111681536-111681757 | Rare:75 |