Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:15675606-15675735 | Common:1; Rare:24 | ||||
chrX:45771241-45771468 | Rare:24 | ||||
chrX:47212825-47213118 | Rare:59; Clinvar:1 | ||||
chrX:47247641-47247879 | Common:1; Rare:78 | ||||
chrX:56564719-56564874 | Rare:27 | ||||
chrX:56564884-56565092 | Rare:43; Clinvar:1 | ||||
chrX:56565324-56565485 | Rare:49; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chrX:73944228-73944367 | Rare:34 | ||||
chrX:78113861-78114154 | Rare:77; Clinvar:2 | ||||
chrX:129984198-129984371 | Rare:15 |