| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:48071891-48071989 | Rare:13 | ||||
| chrX:48508856-48509027 | Rare:34 | ||||
| chrX:48574880-48575235 | Common:3; Rare:87 | ||||
| chrX:48911623-48911715 | Rare:25; Clinvar (benign):4 | ||||
| chrX:49073995-49074219 | Rare:53 | ||||
| chrX:49079842-49079983 | Rare:24 | ||||
| chrX:49186298-49186494 | Common:1; Rare:34 | ||||
| chrX:51893404-51893673 | Common:1; Rare:58 | ||||
| chrX:53082184-53082374 | Common:1; Rare:52 | ||||
| chrX:53422645-53422920 | Common:1; Rare:64 | ||||
| chrX:54043920-54044095 | Rare:29 | ||||
| chrX:54440271-54440481 | Rare:49 | ||||
| chrX:54530064-54530327 | Common:2; Rare:36 | ||||
| chrX:55000194-55000385 | Rare:35 | ||||
| chrX:55161108-55161256 | Rare:42 |