| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:134460050-134460303 | Common:3; Rare:71 | ||||
| chrX:135052076-135052220 | Common:1; Rare:51 | ||||
| chrX:135343950-135344240 | Common:1; Rare:47 | ||||
| chrX:135344626-135344824 | Common:1; Rare:38 | ||||
| chrX:135520483-135520850 | Rare:59 | ||||
| chrX:135973674-135973835 | Rare:59 | ||||
| chrX:135973941-135974034 | Common:1; Rare:24 | ||||
| chrX:135985339-135985526 | Rare:55; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chrX:136169306-136169641 | Common:2; Rare:38 | ||||
| chrX:136196930-136197089 | Rare:30 | ||||
| chrX:136204872-136204928 | Rare:14 | ||||
| chrX:136880701-136880882 | Rare:39 | ||||
| chrX:141177076-141177321 | Common:1; Rare:33 | ||||
| chrX:149540420-149541098 | Common:6; Rare:110 | ||||
| chrX:149542018-149542292 | Rare:38 |