| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:123732956-123733163 | Rare:35; Clinvar (benign):1 | ||||
| chrX:123859684-123860059 | Common:2; Rare:54 | ||||
| chrX:123960628-123960923 | Rare:35 | ||||
| chrX:123961261-123961337 | Common:2; Rare:19 | ||||
| chrX:123961538-123961846 | Rare:43 | ||||
| chrX:123961944-123962093 | Rare:21 | ||||
| chrX:123963080-123963537 | Common:1; Rare:66 | ||||
| chrX:129906073-129906217 | Rare:34 | ||||
| chrX:130110526-130110692 | Common:1; Rare:36 | ||||
| chrX:130165684-130165945 | Rare:51; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130339650-130339965 | Rare:52 | ||||
| chrX:130401850-130402035 | Common:3; Rare:56 | ||||
| chrX:130903179-130903522 | Common:1; Rare:57 | ||||
| chrX:132023145-132023352 | Rare:49 | ||||
| chrX:132218082-132218293 | Rare:26 |