| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:51894821-51895355 | Common:2; Rare:104 | ||||
| chrX:53082022-53082462 | Common:1; Rare:100 | ||||
| chrX:53083288-53083566 | Rare:48 | ||||
| chrX:53422645-53422971 | Common:1; Rare:69 | ||||
| chrX:53431714-53431843 | Rare:16; Clinvar (benign):1 | ||||
| chrX:53431860-53432043 | Rare:28 | ||||
| chrX:53434314-53434461 | Common:1; Rare:38 | ||||
| chrX:53683904-53684475 | Rare:136 | ||||
| chrX:53686267-53686445 | Rare:28 | ||||
| chrX:54043903-54044046 | Rare:28 | ||||
| chrX:54183566-54183709 | Rare:20 | ||||
| chrX:54440235-54440493 | Rare:54 | ||||
| chrX:54530048-54530340 | Common:2; Rare:41 | ||||
| chrX:55000207-55000427 | Common:1; Rare:53 | ||||
| chrX:55160951-55161277 | Common:2; Rare:85 |