Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:47483169-47483259 | Common:2; Rare:14 | ||||
chrX:47659107-47659230 | Rare:37 | ||||
chrX:47836791-47836953 | Common:1; Rare:38 | ||||
chrX:48475877-48476267 | Rare:67 | ||||
chrX:48508880-48509046 | Rare:32 | ||||
chrX:48574869-48574999 | Rare:38 | ||||
chrX:48898066-48898277 | Common:2; Rare:30 | ||||
chrX:48911589-48911719 | Common:1; Rare:31; Clinvar (benign):6 | ||||
chrX:48911932-48912094 | Rare:27 | ||||
chrX:48958355-48958390 | Rare:11 | ||||
chrX:49079788-49079941 | Rare:22 | ||||
chrX:49123723-49123988 | Rare:55 | ||||
chrX:49186304-49186437 | Rare:20 | ||||
chrX:49922404-49922710 | Rare:70 | ||||
chrX:51893269-51893699 | Common:2; Rare:85 |