Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:44542805-44543058 | Common:1; Rare:56 | ||||
chrX:46545377-46545523 | Common:1; Rare:26; Clinvar (benign):1 | ||||
chrX:47144668-47144778 | Rare:20 | ||||
chrX:47145089-47145285 | Rare:30 | ||||
chrX:47232928-47233030 | Rare:22 | ||||
chrX:47483177-47483252 | Common:2; Rare:12 | ||||
chrX:47836784-47836953 | Common:1; Rare:38 | ||||
chrX:48468294-48468491 | Common:1; Rare:25 | ||||
chrX:48574876-48574974 | Rare:30 | ||||
chrX:48597659-48597809 | Rare:17 | ||||
chrX:49079837-49080042 | Rare:31 | ||||
chrX:49123728-49123976 | Rare:52 | ||||
chrX:49186355-49186451 | Common:1; Rare:16 | ||||
chrX:51893272-51893735 | Common:2; Rare:90 | ||||
chrX:53422627-53422944 | Common:1; Rare:76 |