| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:120560924-120561220 | Rare:62 | ||||
| chrX:120561356-120561725 | Common:1; Rare:61 | ||||
| chrX:120603779-120604143 | Rare:66 | ||||
| chrX:120629800-120630390 | Common:5; Rare:117 | ||||
| chrX:123183047-123183975 | Common:4; Rare:219 | ||||
| chrX:123732957-123733190 | Rare:43; Clinvar (benign):1 | ||||
| chrX:123859901-123860053 | Rare:21 | ||||
| chrX:123860080-123860620 | Common:1; Rare:108 | ||||
| chrX:123959393-123959793 | Rare:82 | ||||
| chrX:123960277-123960548 | Rare:31 | ||||
| chrX:123961222-123961328 | Common:2; Rare:23 | ||||
| chrX:123961510-123961828 | Rare:44 | ||||
| chrX:123961853-123962082 | Rare:38 | ||||
| chrX:123963001-123963230 | Common:1; Rare:30 | ||||
| chrX:129522228-129523141 | Common:2; Rare:169 |