| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:107716215-107716856 | Common:1; Rare:113 | ||||
| chrX:107716881-107717192 | Common:2; Rare:35 | ||||
| chrX:107775586-107775979 | Common:1; Rare:62 | ||||
| chrX:107825542-107825877 | Common:2; Rare:31 | ||||
| chrX:108091504-108091819 | Rare:85 | ||||
| chrX:108439499-108440005 | Common:3; Rare:108 | ||||
| chrX:109536715-109536870 | Rare:19 | ||||
| chrX:109537065-109537268 | Common:2; Rare:41 | ||||
| chrX:109732790-109732935 | Common:1; Rare:12 | ||||
| chrX:109733145-109733574 | Common:1; Rare:96 | ||||
| chrX:110317841-110318267 | Rare:117 | ||||
| chrX:110795735-110795958 | Rare:29 | ||||
| chrX:111680984-111681306 | Rare:79; Clinvar (benign):7 | ||||
| chrX:111681530-111681698 | Rare:64 | ||||
| chrX:112840565-112840681 | Rare:20 |