| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:40468280-40468680 | Common:8; Rare:72 | ||||
| chrX:40472019-40472419 | Common:1; Rare:72 | ||||
| chrX:40736424-40736615 | Common:2; Rare:24 | ||||
| chrX:40997095-40997547 | Common:5; Rare:49 | ||||
| chrX:41025940-41026270 | Common:1; Rare:48 | ||||
| chrX:41026703-41027103 | Rare:77 | ||||
| chrX:41084405-41084862 | Common:2; Rare:124 | ||||
| chrX:41276252-41276392 | Rare:17 | ||||
| chrX:41381600-41382000 | Common:4; Rare:80 | ||||
| chrX:41475111-41475394 | Common:1; Rare:35; Clinvar (benign):1 | ||||
| chrX:41475500-41476102 | Common:1; Rare:80; Clinvar (benign):1 | ||||
| chrX:41476117-41476240 | Rare:16 | ||||
| chrX:41478721-41478852 | Common:1; Rare:14 | ||||
| chrX:41718804-41719204 | Rare:62 | ||||
| chrX:41921390-41921790 | Common:2; Rare:88 |