| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:48574869-48575246 | Common:3; Rare:92 | ||||
| chrX:48597225-48597550 | Common:1; Rare:52 | ||||
| chrX:48597680-48597885 | Common:1; Rare:26 | ||||
| chrX:48696579-48696777 | Rare:43 | ||||
| chrX:48898068-48898259 | Common:2; Rare:28 | ||||
| chrX:48911622-48911715 | Rare:25; Clinvar (benign):4 | ||||
| chrX:48918998-48919271 | Rare:47 | ||||
| chrX:48958308-48958531 | Rare:58 | ||||
| chrX:49002189-49002518 | Common:2; Rare:60 | ||||
| chrX:49073995-49074261 | Rare:58 | ||||
| chrX:49079789-49079946 | Rare:22 | ||||
| chrX:49101110-49101411 | Common:2; Rare:62 | ||||
| chrX:49123705-49123988 | Common:1; Rare:61 | ||||
| chrX:49171769-49172013 | Common:3; Rare:30 | ||||
| chrX:49186289-49186416 | Rare:20 |