| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:119574797-119574904 | Common:2; Rare:23 | ||||
| chrX:119791574-119791978 | Common:2; Rare:108 | ||||
| chrX:119852932-119853231 | Common:3; Rare:49; Clinvar (benign):3 | ||||
| chrX:119871621-119871933 | Common:2; Rare:65; Clinvar (benign):3 | ||||
| chrX:120250614-120250864 | Common:3; Rare:42 | ||||
| chrX:120560480-120560859 | Rare:59; Clinvar:2 | ||||
| chrX:120560929-120561146 | Rare:41 | ||||
| chrX:120561395-120561715 | Common:1; Rare:51 | ||||
| chrX:120603797-120604154 | Rare:68 | ||||
| chrX:120604621-120604769 | Rare:15 | ||||
| chrX:120629916-120630266 | Common:4; Rare:67 | ||||
| chrX:123859638-123859864 | Common:1; Rare:31 | ||||
| chrX:123859969-123860270 | Rare:56 | ||||
| chrX:123960350-123960726 | Rare:28 | ||||
| chrX:123961255-123961432 | Common:2; Rare:24 |