| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:119236517-119236572 | Rare:18 | ||||
| chrX:119236575-119236691 | Rare:25 | ||||
| chrX:119399278-119399609 | Common:3; Rare:64 | ||||
| chrX:119468198-119468607 | Common:3; Rare:118 | ||||
| chrX:119469090-119469135 | Rare:10 | ||||
| chrX:119574373-119574610 | Rare:52 | ||||
| chrX:119574811-119574897 | Common:2; Rare:15 | ||||
| chrX:119606391-119606583 | Common:1; Rare:35 | ||||
| chrX:119791572-119791994 | Common:2; Rare:112 | ||||
| chrX:119852921-119853285 | Common:3; Rare:58; Clinvar (benign):3 | ||||
| chrX:119871536-119872013 | Common:3; Rare:89; Clinvar (benign):4 | ||||
| chrX:119943607-119943852 | Rare:44 | ||||
| chrX:120250824-120250905 | Rare:10 | ||||
| chrX:120560524-120560860 | Rare:53; Clinvar:1 | ||||
| chrX:120604047-120604154 | Rare:23 |