| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:41335014-41335124 | Common:1; Rare:17 | ||||
| chrX:41923359-41923859 | Common:9; Rare:200 | ||||
| chrX:43655734-43656551 | Rare:168 | ||||
| chrX:44542792-44543165 | Common:2; Rare:123 | ||||
| chrX:44872803-44873306 | Common:1; Rare:137 | ||||
| chrX:46447150-46447349 | Rare:72 | ||||
| chrX:46545341-46545583 | Common:2; Rare:96; Clinvar (benign):2 | ||||
| chrX:46836695-46837081 | Rare:138; Clinvar:6; Clinvar (benign):2 | ||||
| chrX:46912342-46912667 | Rare:143 | ||||
| chrX:47078246-47078513 | Common:5; Rare:57 | ||||
| chrX:47078680-47079092 | Common:6; Rare:97 | ||||
| chrX:47144487-47144837 | Common:2; Rare:99; Clinvar (benign):1 | ||||
| chrX:47145043-47145329 | Rare:79 | ||||
| chrX:47190647-47190941 | Rare:82 | ||||
| chrX:47218665-47218802 | Rare:119 |