| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:118975191-118975411 | Common:1; Rare:61 | ||||
| chrX:119236161-119236375 | Rare:55 | ||||
| chrX:119236551-119236670 | Rare:32 | ||||
| chrX:119468198-119468506 | Common:3; Rare:103 | ||||
| chrX:119574364-119574634 | Rare:56 | ||||
| chrX:119574658-119574904 | Common:2; Rare:53 | ||||
| chrX:119791563-119791994 | Common:2; Rare:113 | ||||
| chrX:119871621-119871987 | Common:2; Rare:73; Clinvar (benign):3 | ||||
| chrX:119943579-119943852 | Rare:50 | ||||
| chrX:120559889-120560126 | Rare:36 | ||||
| chrX:120560923-120561194 | Rare:57 | ||||
| chrX:120561388-120561712 | Common:1; Rare:52 | ||||
| chrX:120603869-120604010 | Rare:29 | ||||
| chrX:120604029-120604157 | Rare:28 | ||||
| chrX:120604623-120604770 | Rare:15 |