| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:123961543-123961849 | Rare:44 | ||||
| chrX:129906073-129906191 | Rare:30 | ||||
| chrX:131058149-131058394 | Common:1; Rare:37 | ||||
| chrX:132023145-132023345 | Rare:49 | ||||
| chrX:132219427-132219475 | Rare:1 | ||||
| chrX:134373162-134373402 | Common:4; Rare:59 | ||||
| chrX:135022469-135022706 | Rare:52 | ||||
| chrX:135344601-135344816 | Common:2; Rare:38 | ||||
| chrX:135973717-135973835 | Rare:42 | ||||
| chrX:139222719-139222986 | Rare:23 | ||||
| chrX:141177076-141177289 | Common:1; Rare:26 | ||||
| chrX:149540909-149541087 | Common:3; Rare:32 | ||||
| chrX:149938444-149938637 | Common:1; Rare:47 | ||||
| chrX:150568318-150568653 | Common:1; Rare:69; Clinvar (benign):1 | ||||
| chrX:150898590-150898911 | Common:3; Rare:91 |