| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:101348680-101348781 | Common:3; Rare:17 | ||||
| chrX:101386143-101386353 | Rare:23 | ||||
| chrX:101390897-101391326 | Common:1; Rare:103 | ||||
| chrX:101407739-101407828 | Rare:8; Clinvar (benign):3 | ||||
| chrX:101407841-101408478 | Common:5; Rare:125; Clinvar:2; Clinvar (benign):11 | ||||
| chrX:101417966-101418131 | Common:1; Rare:17 | ||||
| chrX:101418214-101418418 | Common:2; Rare:39 | ||||
| chrX:101485306-101485530 | Rare:28 | ||||
| chrX:102125360-102125776 | Common:2; Rare:77 | ||||
| chrX:102142399-102142727 | Common:1; Rare:71 | ||||
| chrX:102651318-102651523 | Common:2; Rare:59 | ||||
| chrX:102712369-102712457 | Rare:22 | ||||
| chrX:103093115-103093329 | Common:1; Rare:27 | ||||
| chrX:103214951-103215164 | Common:2; Rare:46 | ||||
| chrX:103276697-103276903 | Rare:23 |