| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:16870313-16870621 | Common:2; Rare:79 | ||||
| chrX:18983998-18984203 | Rare:44 | ||||
| chrX:19343701-19344046 | Common:6; Rare:96; Clinvar (benign):1 | ||||
| chrX:23667701-23667803 | Rare:26 | ||||
| chrX:23782948-23783423 | Common:5; Rare:104 | ||||
| chrX:23785320-23785828 | Common:1; Rare:83 | ||||
| chrX:23907698-23907792 | Common:1; Rare:23 | ||||
| chrX:23907865-23908068 | Rare:42 | ||||
| chrX:24054884-24055028 | Rare:51 | ||||
| chrX:24693822-24693956 | Common:1; Rare:26 | ||||
| chrX:30653112-30653549 | Common:2; Rare:113 | ||||
| chrX:40580754-40581033 | Common:5; Rare:71; Clinvar (benign):3 | ||||
| chrX:40659306-40659581 | Rare:37 | ||||
| chrX:41086040-41086090 | Common:1; Rare:6 | ||||
| chrX:41688673-41689080 | Common:2; Rare:47 |