| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:119574367-119574594 | Rare:52 | ||||
| chrX:119791596-119791979 | Common:2; Rare:101 | ||||
| chrX:119871643-119871891 | Common:1; Rare:52; Clinvar (benign):2 | ||||
| chrX:120604032-120604144 | Rare:21 | ||||
| chrX:123733025-123733146 | Rare:19 | ||||
| chrX:129906078-129906197 | Rare:27 | ||||
| chrX:135973738-135973827 | Rare:35 | ||||
| chrX:141177085-141177290 | Rare:25 | ||||
| chrX:150983077-150983368 | Common:2; Rare:58 | ||||
| chrX:152698648-152698816 | Rare:2 | ||||
| chrX:152733669-152733849 | Common:1; Rare:56 | ||||
| chrX:152769676-152769801 | |||||
| chrX:152830712-152831066 | Common:2; Rare:65 | ||||
| chrX:153794322-153794682 | Common:1; Rare:110; Clinvar (benign):2 | ||||
| chrX:153971181-153971274 | Rare:24 |