| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:24025663-24025774 | Rare:25 | ||||
| chrX:34656433-34656765 | Rare:47 | ||||
| chrX:47214544-47214854 | Common:1; Rare:57; Clinvar (benign):1 | ||||
| chrX:63426878-63426941 | Rare:12 | ||||
| chrX:72129603-72129781 | Common:1; Rare:24 | ||||
| chrX:73827184-73827362 | Common:1; Rare:44 | ||||
| chrX:74254180-74254415 | Common:2; Rare:31 | ||||
| chrX:74292343-74292743 | Rare:63 | ||||
| chrX:74420682-74420939 | Common:1; Rare:59 | ||||
| chrX:103215994-103216202 | Rare:33 | ||||
| chrX:103536076-103536392 | Common:1; Rare:31 | ||||
| chrX:107676946-107677165 | Rare:27 | ||||
| chrX:115562697-115562798 | Rare:10 | ||||
| chrX:120245202-120245374 | Common:2; Rare:25 | ||||
| chrX:124242837-124243061 | Common:2; Rare:24 |