| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrM:12627-13088 | |||||
| chrM:13970-14368 | |||||
| chrX:1392042-1392406 | Common:6; Rare:165 | ||||
| chrX:2691030-2691370 | Common:13; Rare:122 | ||||
| chrX:2691423-2691520 | Common:1; Rare:61 | ||||
| chrX:2828617-2829000 | Common:3; Rare:59; Clinvar (benign):1 | ||||
| chrX:2929254-2929513 | Common:2; Rare:71 | ||||
| chrX:7927337-7927484 | Common:1; Rare:38 | ||||
| chrX:7927695-7927801 | Rare:24 | ||||
| chrX:10620447-10620689 | Common:1; Rare:35 | ||||
| chrX:11111131-11111382 | Common:4; Rare:54 | ||||
| chrX:11265878-11266089 | Common:4; Rare:42 | ||||
| chrX:12791262-12791447 | Rare:27 | ||||
| chrX:13652983-13653188 | Rare:47 | ||||
| chrX:13688995-13689269 | Common:2; Rare:76 |