| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:120559857-120560124 | Rare:44 | ||||
| chrX:120560366-120560863 | Rare:83; Clinvar:2 | ||||
| chrX:120603996-120604195 | Rare:37 | ||||
| chrX:123733025-123733156 | Rare:21 | ||||
| chrX:123859717-123860053 | Common:2; Rare:49 | ||||
| chrX:130110490-130110677 | Common:1; Rare:39 | ||||
| chrX:130165826-130165945 | Rare:18; Clinvar (benign):1 | ||||
| chrX:149540435-149540730 | Common:1; Rare:36 | ||||
| chrX:149540811-149541048 | Common:4; Rare:45 | ||||
| chrX:149938414-149938622 | Common:1; Rare:54 | ||||
| chrX:151397054-151397241 | Common:4; Rare:95 | ||||
| chrX:152830717-152831112 | Common:2; Rare:70 | ||||
| chrX:153599090-153599391 | Common:14; Rare:64 | ||||
| chrX:153724343-153724490 | Common:1; Rare:38 | ||||
| chrX:153794324-153794668 | Common:1; Rare:110; Clinvar (benign):2 |