| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:119574374-119574599 | Rare:51 | ||||
| chrX:119791585-119791732 | Rare:62 | ||||
| chrX:119852924-119853276 | Common:3; Rare:57; Clinvar (benign):3 | ||||
| chrX:119871573-119871942 | Common:2; Rare:72; Clinvar (benign):3 | ||||
| chrX:119943597-119943852 | Rare:44 | ||||
| chrX:120250582-120250942 | Common:4; Rare:58 | ||||
| chrX:120469144-120469442 | Common:1; Rare:60; Clinvar:8; Clinvar (benign):4 | ||||
| chrX:120560951-120561199 | Rare:46 | ||||
| chrX:120603797-120604150 | Rare:66 | ||||
| chrX:120604482-120604772 | Rare:33 | ||||
| chrX:120629940-120630326 | Common:4; Rare:76 | ||||
| chrX:123733025-123733152 | Rare:20 | ||||
| chrX:123859650-123859864 | Common:1; Rare:31 | ||||
| chrX:123960350-123960752 | Rare:31 | ||||
| chrX:123961243-123961435 | Common:2; Rare:26 |