| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:119468209-119468572 | Common:3; Rare:110 | ||||
| chrX:119469043-119469215 | Rare:49 | ||||
| chrX:119574355-119574581 | Rare:51 | ||||
| chrX:119791606-119791958 | Common:2; Rare:88 | ||||
| chrX:119852924-119853276 | Common:3; Rare:57; Clinvar (benign):3 | ||||
| chrX:119871622-119871927 | Common:2; Rare:63; Clinvar (benign):3 | ||||
| chrX:120560480-120560860 | Rare:60; Clinvar:2 | ||||
| chrX:120560929-120561143 | Rare:40 | ||||
| chrX:120561404-120561603 | Common:1; Rare:35 | ||||
| chrX:120629938-120630227 | Common:4; Rare:55 | ||||
| chrX:123960340-123960726 | Rare:30 | ||||
| chrX:123961290-123961432 | Common:2; Rare:21 | ||||
| chrX:129779817-129779980 | Rare:22 | ||||
| chrX:129905941-129906201 | Rare:68 | ||||
| chrX:130401895-130402015 | Common:2; Rare:36 |