| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:123733025-123733152 | Rare:20 | ||||
| chrX:129654539-129654741 | Common:1; Rare:45 | ||||
| chrX:129906073-129906213 | Rare:33 | ||||
| chrX:130165703-130165903 | Rare:39; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:132219439-132219510 | Rare:5 | ||||
| chrX:134460055-134460303 | Common:3; Rare:69 | ||||
| chrX:134915198-134915261 | Rare:4 | ||||
| chrX:135022468-135022560 | Rare:32 | ||||
| chrX:135344022-135344215 | Common:1; Rare:32 | ||||
| chrX:135344596-135344818 | Common:2; Rare:39 | ||||
| chrX:135973703-135973841 | Rare:51 | ||||
| chrX:135985344-135985504 | Rare:47; Clinvar (benign):4 | ||||
| chrX:139204932-139205161 | Common:1; Rare:34 | ||||
| chrX:141177026-141177325 | Common:1; Rare:46 | ||||
| chrX:149540811-149541048 | Common:4; Rare:45 |