Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:24054870-24054971 | Rare:30 | ||||
chrX:24693795-24693956 | Common:1; Rare:28 | ||||
chrX:30653164-30653429 | Common:2; Rare:71 | ||||
chrX:44542820-44543056 | Common:1; Rare:45 | ||||
chrX:46545377-46545534 | Common:1; Rare:30; Clinvar (benign):1 | ||||
chrX:47144636-47144867 | Common:1; Rare:39 | ||||
chrX:47144995-47145295 | Rare:40 | ||||
chrX:47482567-47482664 | Common:5; Rare:21; Clinvar:2 | ||||
chrX:47836791-47836924 | Common:1; Rare:35 | ||||
chrX:48574869-48574981 | Rare:33 | ||||
chrX:48683516-48683861 | Rare:50 | ||||
chrX:48911637-48911715 | Rare:19; Clinvar (benign):3 | ||||
chrX:48919019-48919297 | Rare:43 | ||||
chrX:48958320-48958415 | Rare:27 | ||||
chrX:49171769-49171974 | Common:3; Rare:24 |