Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:153864975-153865113 | Common:1; Rare:37; Clinvar:1; Clinvar (benign):2 | ||||
chrX:153934957-153935349 | Common:1; Rare:93 | ||||
chrX:153971191-153971341 | Rare:39 | ||||
chrX:154019824-154020052 | Rare:47 | ||||
chrX:154398822-154399021 | Common:2; Rare:42 | ||||
chrX:154409205-154409427 | Rare:35 | ||||
chrX:154428462-154428806 | Common:3; Rare:72; Clinvar:1 | ||||
chrX:154547550-154547645 | Common:1; Rare:24; Clinvar (benign):1 | ||||
chrX:155026891-155026951 | Rare:17 | ||||
chrX:155026974-155027059 | Rare:24 | ||||
chrX:155071066-155071533 | Common:1; Rare:100 | ||||
chrY:19744712-19745011 | Rare:3 |