Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:63432392-63432433 | Rare:12 | ||||
chrX:65524732-65525048 | Rare:32 | ||||
chrX:67545564-67545702 | Rare:33; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chrX:70137577-70137642 | Common:1; Rare:11 | ||||
chrX:70963272-70963316 | Rare:3 | ||||
chrX:71290021-71290340 | Rare:42 | ||||
chrX:71298724-71298896 | Common:1; Rare:32 | ||||
chrX:71544442-71544634 | Rare:20 | ||||
chrX:72275131-72275236 | Rare:19 | ||||
chrX:73820691-73820905 | Rare:50 | ||||
chrX:73821079-73821351 | Common:1; Rare:54 | ||||
chrX:73822064-73822186 | Common:1; Rare:23 | ||||
chrX:73822268-73822620 | Common:1; Rare:86 | ||||
chrX:73822627-73822933 | Common:1; Rare:74 | ||||
chrX:73823188-73823340 | Common:7; Rare:34 |