| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:130165657-130165918 | Rare:51; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:131058165-131058346 | Common:1; Rare:26 | ||||
| chrX:132023145-132023305 | Rare:41 | ||||
| chrX:132218160-132218308 | Rare:26 | ||||
| chrX:132219391-132219559 | Rare:20 | ||||
| chrX:133985274-133985666 | Common:1; Rare:70; Clinvar:2; Clinvar (benign):7 | ||||
| chrX:135022468-135022663 | Rare:47 | ||||
| chrX:135032181-135032380 | Rare:46 | ||||
| chrX:135344005-135344218 | Common:1; Rare:35 | ||||
| chrX:135344578-135344823 | Common:2; Rare:44 | ||||
| chrX:135973671-135973872 | Rare:67 | ||||
| chrX:135985344-135985537 | Rare:61; Clinvar:1; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chrX:136497076-136497438 | Common:3; Rare:93 | ||||
| chrX:139933025-139933210 | Rare:36 | ||||
| chrX:141177030-141177314 | Common:1; Rare:43 |