| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:19343691-19344024 | Common:6; Rare:95; Clinvar (benign):1 | ||||
| chrX:19670887-19670979 | Rare:19 | ||||
| chrX:23782896-23783213 | Common:5; Rare:68 | ||||
| chrX:23907714-23908006 | Common:1; Rare:60 | ||||
| chrX:37349076-37349381 | Common:2; Rare:43 | ||||
| chrX:40735820-40736020 | Common:1; Rare:37 | ||||
| chrX:46545409-46545532 | Rare:23 | ||||
| chrX:47144906-47145206 | Rare:33 | ||||
| chrX:47232914-47233032 | Rare:32 | ||||
| chrX:47561058-47561227 | Rare:29 | ||||
| chrX:47659079-47659235 | Rare:46 | ||||
| chrX:48475897-48476249 | Rare:62 | ||||
| chrX:48574869-48574986 | Rare:34 | ||||
| chrX:48696587-48696756 | Rare:37 | ||||
| chrX:49079854-49080005 | Rare:24 |