Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:21940607-21940842 | Common:2; Rare:62 | ||||
chrX:23667340-23667571 | Common:2; Rare:75 | ||||
chrX:23907838-23908068 | Rare:43 | ||||
chrX:24054914-24055000 | Rare:37 | ||||
chrX:40735910-40736027 | Rare:17 | ||||
chrX:41334064-41334185 | Common:1; Rare:25 | ||||
chrX:44542828-44543090 | Common:1; Rare:50 | ||||
chrX:46545413-46545520 | Rare:17 | ||||
chrX:47144654-47144846 | Common:1; Rare:34 | ||||
chrX:47145043-47145291 | Rare:36 | ||||
chrX:47560959-47561239 | Common:1; Rare:51 | ||||
chrX:48476135-48476261 | Rare:28 | ||||
chrX:48508894-48508992 | Rare:14 | ||||
chrX:48574869-48574956 | Rare:26 | ||||
chrX:48911637-48911715 | Rare:19; Clinvar (benign):3 |