Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:23907694-23908054 | Common:1; Rare:80 | ||||
chrX:24054888-24054992 | Rare:39 | ||||
chrX:30653171-30653425 | Common:2; Rare:69 | ||||
chrX:33211396-33211661 | Common:1; Rare:42; Clinvar:4; Clinvar (benign):2 | ||||
chrX:37349189-37349386 | Common:2; Rare:29 | ||||
chrX:40580700-40581015 | Common:4; Rare:71 | ||||
chrX:46545377-46545520 | Common:1; Rare:25; Clinvar (benign):1 | ||||
chrX:47144654-47144816 | Common:1; Rare:27 | ||||
chrX:47145043-47145301 | Rare:36 | ||||
chrX:47482571-47482664 | Common:5; Rare:19; Clinvar:2 | ||||
chrX:47483169-47483277 | Common:3; Rare:14 | ||||
chrX:47659004-47659267 | Rare:72 | ||||
chrX:47836791-47836953 | Common:1; Rare:38 | ||||
chrX:48476080-48476231 | Rare:28 | ||||
chrX:49079831-49079975 | Rare:22 |