| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:106007820-106008220 | Rare:84 | ||||
| chrX:118156240-118156661 | Rare:128 | ||||
| chrX:118839390-118839579 | Rare:41 | ||||
| chrX:119841051-119841651 | Rare:116; Clinvar:1; Clinvar (benign):1 | ||||
| chrX:120287570-120288190 | Rare:125 | ||||
| chrX:120752670-120753130 | Common:5; Rare:112 | ||||
| chrX:123764980-123765340 | Common:1; Rare:74 | ||||
| chrX:123780433-123780787 | Common:18; Rare:104 | ||||
| chrX:123822990-123823360 | Common:1; Rare:33 | ||||
| chrX:123824860-123825280 | Rare:71 | ||||
| chrX:123830249-123830740 | Common:5; Rare:90 | ||||
| chrX:129144577-129144997 | Common:3; Rare:95 | ||||
| chrX:129777266-129777666 | Common:8; Rare:118 | ||||
| chrX:130071570-130072060 | Common:1; Rare:78 | ||||
| chrX:130386343-130386555 | Common:1; Rare:51 |