Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:55453053-55453158 | Rare:18 | ||||
chrX:55453175-55453242 | Rare:11 | ||||
chrX:55453286-55453390 | Rare:12 | ||||
chrX:56564190-56564370 | Rare:34 | ||||
chrX:56564729-56564766 | Rare:7 | ||||
chrX:56564835-56564894 | Rare:16 | ||||
chrX:56565101-56565482 | Rare:89; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chrX:56565739-56565867 | Rare:31; Clinvar:2 | ||||
chrX:56565901-56566156 | Rare:22 | ||||
chrX:56566767-56566812 | Rare:4 | ||||
chrX:63350143-63350366 | Rare:36 | ||||
chrX:63350392-63350530 | Rare:27 | ||||
chrX:63428239-63428405 | Rare:20 | ||||
chrX:63428712-63428769 | Rare:7 | ||||
chrX:63429309-63429405 | Rare:22 |