| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:119758415-119758596 | Common:2; Rare:27 | ||||
| chrX:119791626-119791704 | Rare:27 | ||||
| chrX:119871666-119871891 | Common:1; Rare:50; Clinvar (benign):2 | ||||
| chrX:120559896-120560077 | Rare:30 | ||||
| chrX:120604032-120604192 | Rare:31 | ||||
| chrX:120630037-120630357 | Common:4; Rare:70 | ||||
| chrX:123732958-123733121 | Rare:29; Clinvar (benign):1 | ||||
| chrX:123960242-123960558 | Rare:37 | ||||
| chrX:123960636-123960876 | Rare:28 | ||||
| chrX:123961260-123961331 | Common:2; Rare:18 | ||||
| chrX:123961957-123962081 | Rare:18 | ||||
| chrX:123963164-123963439 | Common:1; Rare:38 | ||||
| chrX:129779784-129780140 | Rare:60 | ||||
| chrX:130110474-130110634 | Rare:38 | ||||
| chrX:130165826-130166109 | Rare:51; Clinvar (benign):1 |