| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:38220696-38221047 | Common:3; Rare:96 | ||||
| chrX:40580680-40581055 | Common:5; Rare:86; Clinvar (benign):3 | ||||
| chrX:41085201-41085388 | Common:2; Rare:44 | ||||
| chrX:41333208-41333540 | Rare:67 | ||||
| chrX:41334985-41335136 | Common:1; Rare:19 | ||||
| chrX:41688947-41689070 | Common:1; Rare:9 | ||||
| chrX:43656083-43656421 | Rare:61 | ||||
| chrX:43743585-43743885 | Common:2; Rare:34 | ||||
| chrX:43882396-43882554 | Common:1; Rare:46 | ||||
| chrX:44542828-44543056 | Common:1; Rare:43 | ||||
| chrX:44873468-44873629 | Rare:51; Clinvar (benign):1 | ||||
| chrX:44874080-44874204 | Common:1; Rare:25 | ||||
| chrX:45200929-45201259 | Common:1; Rare:35 | ||||
| chrX:46545380-46545574 | Rare:46 | ||||
| chrX:47144668-47144816 | Common:1; Rare:24 |