| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:119791626-119791971 | Common:2; Rare:82 | ||||
| chrX:119871702-119871891 | Common:1; Rare:47; Clinvar (benign):2 | ||||
| chrX:120604010-120604202 | Rare:38 | ||||
| chrX:120604620-120604732 | Rare:9 | ||||
| chrX:120630013-120630369 | Common:4; Rare:76 | ||||
| chrX:123960630-123960732 | Rare:10 | ||||
| chrX:123961261-123961323 | Common:2; Rare:17 | ||||
| chrX:123961563-123961860 | Rare:41 | ||||
| chrX:123963178-123963444 | Common:1; Rare:34 | ||||
| chrX:129779788-129780148 | Rare:61 | ||||
| chrX:130110460-130110677 | Common:1; Rare:45 | ||||
| chrX:130165839-130165935 | Rare:12; Clinvar (benign):1 | ||||
| chrX:132218083-132218282 | Rare:22 | ||||
| chrX:135032109-135032365 | Common:1; Rare:52 | ||||
| chrX:135973637-135973756 | Rare:34 |