| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:47483169-47483277 | Common:3; Rare:14 | ||||
| chrX:48508870-48509036 | Rare:30 | ||||
| chrX:48574694-48575210 | Common:3; Rare:144 | ||||
| chrX:48911613-48911715 | Rare:27; Clinvar (benign):4 | ||||
| chrX:49002204-49002345 | Rare:38 | ||||
| chrX:49079842-49079937 | Rare:13 | ||||
| chrX:49171769-49171951 | Common:3; Rare:21 | ||||
| chrX:53422624-53422776 | Rare:43 | ||||
| chrX:53434335-53434569 | Common:1; Rare:51 | ||||
| chrX:53683881-53684292 | Rare:102 | ||||
| chrX:54440271-54440433 | Rare:28 | ||||
| chrX:54440547-54440724 | Common:1; Rare:24 | ||||
| chrX:54530040-54530294 | Common:2; Rare:37 | ||||
| chrX:55000204-55000385 | Rare:34 | ||||
| chrX:55161159-55161246 | Rare:22 |