| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:119791584-119791978 | Common:2; Rare:107 | ||||
| chrX:119852924-119853276 | Common:3; Rare:57; Clinvar (benign):3 | ||||
| chrX:119871609-119871987 | Common:2; Rare:74; Clinvar (benign):3 | ||||
| chrX:119895781-119895937 | Rare:15 | ||||
| chrX:119896077-119896256 | Rare:9 | ||||
| chrX:119943584-119943852 | Rare:50 | ||||
| chrX:120250550-120250949 | Common:4; Rare:63 | ||||
| chrX:120559857-120560144 | Rare:48 | ||||
| chrX:120560656-120560863 | Rare:34 | ||||
| chrX:120560880-120561107 | Rare:44 | ||||
| chrX:120575756-120575953 | Rare:25 | ||||
| chrX:120604364-120604776 | Rare:55 | ||||
| chrX:120629916-120630159 | Common:1; Rare:44 | ||||
| chrX:123733018-123733105 | Rare:15 | ||||
| chrX:123859589-123860273 | Common:2; Rare:109 |