Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:46545377-46545547 | Common:1; Rare:35; Clinvar (benign):1 | ||||
chrX:47144680-47144813 | Rare:21 | ||||
chrX:47202218-47202502 | Rare:65; Clinvar:2; Clinvar (benign):3 | ||||
chrX:47659101-47659284 | Rare:51 | ||||
chrX:48475891-48476239 | Rare:59 | ||||
chrX:48508856-48509030 | Rare:35 | ||||
chrX:48574860-48574983 | Rare:36 | ||||
chrX:48958367-48958625 | Rare:52 | ||||
chrX:49123725-49123963 | Rare:52 | ||||
chrX:55000134-55000393 | Common:1; Rare:45 | ||||
chrX:68498984-68499063 | Rare:19 | ||||
chrX:70289875-70290120 | Rare:46 | ||||
chrX:74614581-74614728 | Rare:24 | ||||
chrX:75274640-75274736 | Common:1; Rare:16 | ||||
chrX:77895392-77895750 | Rare:104; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 |