| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:153904519-153904696 | Rare:33 | ||||
| chrX:153944599-153944749 | Common:2; Rare:36 | ||||
| chrX:153970905-153970974 | Rare:16 | ||||
| chrX:153971168-153971264 | Rare:20 | ||||
| chrX:153972403-153972782 | Common:2; Rare:117 | ||||
| chrX:154351864-154352448 | Common:3; Rare:115; Clinvar:12; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chrX:154352979-154353461 | Common:3; Rare:119; Clinvar:10; Clinvar (benign):11 | ||||
| chrX:154353904-154354712 | Common:3; Rare:175; Clinvar:8; Clinvar (benign):21 | ||||
| chrX:154358197-154358576 | Common:3; Rare:83; Clinvar:4; Clinvar (benign):17; Clinvar (pathogenic):1 | ||||
| chrX:154359244-154359918 | Common:1; Rare:158; Clinvar:15; Clinvar (benign):19; Clinvar (pathogenic):1 | ||||
| chrX:154364908-154365265 | Common:2; Rare:100; Clinvar:8; Clinvar (benign):8 | ||||
| chrX:154374505-154374892 | Common:2; Rare:74 | ||||
| chrX:154409148-154409427 | Rare:46 | ||||
| chrX:154428457-154428695 | Common:2; Rare:41 | ||||
| chrX:154486574-154486762 | Rare:30 |