| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:38220740-38220945 | Common:1; Rare:53 | ||||
| chrX:38327471-38327682 | Rare:53 | ||||
| chrX:38561265-38561582 | Common:3; Rare:80; Clinvar (benign):1 | ||||
| chrX:38801192-38801470 | Common:1; Rare:56 | ||||
| chrX:40580639-40581049 | Common:5; Rare:90; Clinvar (benign):3 | ||||
| chrX:40735297-40735690 | Rare:99 | ||||
| chrX:41085997-41086082 | Common:1; Rare:21 | ||||
| chrX:41333870-41333975 | Common:2; Rare:31 | ||||
| chrX:41334969-41335220 | Common:2; Rare:41 | ||||
| chrX:41688943-41689084 | Common:1; Rare:13 | ||||
| chrX:43656024-43656371 | Rare:59 | ||||
| chrX:46447188-46447341 | Rare:28 | ||||
| chrX:46545368-46545544 | Common:1; Rare:36; Clinvar (benign):1 | ||||
| chrX:46912273-46912328 | Rare:10 | ||||
| chrX:46912472-46912691 | Rare:53 |