| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:119468216-119468506 | Common:3; Rare:97 | ||||
| chrX:119574387-119574575 | Rare:41 | ||||
| chrX:119871682-119871891 | Common:1; Rare:50; Clinvar (benign):2 | ||||
| chrX:120560477-120560860 | Rare:61; Clinvar:2 | ||||
| chrX:120604006-120604201 | Rare:37 | ||||
| chrX:130110495-130110677 | Common:1; Rare:39 | ||||
| chrX:134796278-134796411 | Common:1; Rare:6 | ||||
| chrX:135052112-135052290 | Common:2; Rare:51 | ||||
| chrX:141177076-141177299 | Common:1; Rare:28 | ||||
| chrX:149540447-149540731 | Common:1; Rare:34 | ||||
| chrX:149540909-149541031 | Common:2; Rare:21 | ||||
| chrX:149938437-149938540 | Common:1; Rare:30 | ||||
| chrX:151396964-151397239 | Common:5; Rare:124 | ||||
| chrX:152830716-152831106 | Common:2; Rare:69 | ||||
| chrX:153599108-153599356 | Common:13; Rare:49 |