Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:47129499-47129606 | Common:2; Rare:15 | ||||
chrX:48787921-48788036 | Rare:17 | ||||
chrX:49156245-49156355 | Rare:21 | ||||
chrX:49173138-49173422 | Rare:64 | ||||
chrX:49231001-49231217 | Common:1; Rare:38 | ||||
chrX:55908044-55908256 | Rare:38 | ||||
chrX:56564414-56564460 | Common:1; Rare:6; Clinvar (benign):1 | ||||
chrX:56564735-56564872 | Rare:22 | ||||
chrX:63350650-63350749 | Common:1; Rare:16 | ||||
chrX:66015236-66015483 | Common:2; Rare:39 | ||||
chrX:73944107-73944351 | Common:1; Rare:63 | ||||
chrX:74292513-74292744 | Rare:40 | ||||
chrX:78113862-78114103 | Rare:66; Clinvar:2 | ||||
chrX:78653333-78653462 | Common:1; Rare:17 | ||||
chrX:103215899-103216290 | Common:1; Rare:74 |