Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:51698434-51698744 | Rare:99 | ||||
chr10:61903054-61903357 | Common:1; Rare:81 | ||||
chr10:68965140-68965485 | Common:2; Rare:51 | ||||
chr10:68973302-68973664 | Common:1; Rare:59 | ||||
chr10:71965256-71965381 | Common:1; Rare:29 | ||||
chr10:73247247-73247409 | Rare:89 | ||||
chr10:73730452-73730585 | Common:1; Rare:36 | ||||
chr10:74070900-74071087 | Rare:40; Clinvar:1; Clinvar (benign):3 | ||||
chr10:74095435-74095835 | Rare:91; Clinvar:7; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
chr10:74103545-74103927 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):3 | ||||
chr10:74110761-74111012 | Common:1; Rare:42 | ||||
chr10:74112584-74113047 | Common:3; Rare:79 | ||||
chr10:74114586-74114894 | Common:1; Rare:52; Clinvar:2; Clinvar (benign):2 | ||||
chr10:75230780-75230930 | Common:1; Rare:39 | ||||
chr10:75409572-75409884 | Common:4; Rare:79 |