| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:109536689-109536861 | Rare:20 | ||||
| chrX:109537063-109537237 | Common:1; Rare:37 | ||||
| chrX:109733185-109733479 | Common:1; Rare:67 | ||||
| chrX:110002671-110002725 | Rare:11 | ||||
| chrX:110317898-110318277 | Rare:98 | ||||
| chrX:111681031-111681270 | Rare:65; Clinvar (benign):6 | ||||
| chrX:118345859-118346155 | Common:3; Rare:50 | ||||
| chrX:119468205-119468506 | Common:3; Rare:99 | ||||
| chrX:119574364-119574602 | Rare:55 | ||||
| chrX:119791566-119791978 | Common:2; Rare:109 | ||||
| chrX:119852915-119853276 | Common:3; Rare:58; Clinvar (benign):3 | ||||
| chrX:119871621-119871909 | Common:2; Rare:61; Clinvar (benign):3 | ||||
| chrX:119943696-119943902 | Rare:34 | ||||
| chrX:120604061-120604147 | Rare:19 | ||||
| chrX:120630008-120630266 | Common:3; Rare:51 |