| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:119565353-119565499 | Common:3; Rare:34 | ||||
| chrX:119574373-119574581 | Rare:47 | ||||
| chrX:119574668-119574910 | Common:2; Rare:52 | ||||
| chrX:119791572-119791978 | Common:2; Rare:108 | ||||
| chrX:119871621-119871920 | Common:2; Rare:61; Clinvar (benign):3 | ||||
| chrX:120560722-120560860 | Rare:20 | ||||
| chrX:120604009-120604154 | Rare:28 | ||||
| chrX:123733018-123733114 | Rare:17 | ||||
| chrX:123859669-123860109 | Common:2; Rare:65 | ||||
| chrX:123961264-123961432 | Common:2; Rare:22 | ||||
| chrX:123961511-123961850 | Rare:47 | ||||
| chrX:129906031-129906205 | Rare:46 | ||||
| chrX:132023145-132023338 | Rare:49 | ||||
| chrX:135032077-135032386 | Common:1; Rare:66 | ||||
| chrX:135344027-135344240 | Common:1; Rare:37 |