Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:369370-369476 | Rare:25 | ||||
chrX:370589-370853 | Common:1; Rare:78 | ||||
chrX:2321432-2321639 | Common:3; Rare:55 | ||||
chrX:2609162-2609425 | Rare:83 | ||||
chrX:10127126-10127295 | Common:4; Rare:23 | ||||
chrX:11351625-11351969 | Common:4; Rare:44 | ||||
chrX:38870553-38870747 | Common:4; Rare:31 | ||||
chrX:38870756-38870825 | Rare:7 | ||||
chrX:43736205-43736249 | Rare:7 | ||||
chrX:47224695-47224849 | Rare:30 | ||||
chrX:53287924-53287944 | Rare:4 | ||||
chrX:53405529-53405815 | Rare:36; Clinvar (benign):2 | ||||
chrX:56564222-56564473 | Common:1; Rare:46; Clinvar (benign):1 | ||||
chrX:67545517-67545712 | Rare:44; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chrX:107676950-107677135 | Rare:23 |