Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:47339322-47339791 | Common:2; Rare:122; Clinvar:10; Clinvar (benign):10; Clinvar (pathogenic):3 | ||||
chr11:47346187-47346656 | Common:3; Rare:124; Clinvar:19; Clinvar (benign):11; Clinvar (pathogenic):12 | ||||
chr11:47347025-47347031 | Rare:1; Clinvar (pathogenic):1 | ||||
chr11:47349772-47350080 | Common:4; Rare:118; Clinvar:28; Clinvar (benign):21; Clinvar (pathogenic):5 | ||||
chr11:47351765-47352049 | Common:1; Rare:52 | ||||
chr11:47420380-47420433 | Rare:9 | ||||
chr11:59560947-59561097 | Common:2; Rare:33 | ||||
chr11:65420019-65420158 | Rare:35 | ||||
chr11:65422657-65422995 | Common:3; Rare:100 | ||||
chr11:65425376-65425600 | Rare:41 | ||||
chr11:65455120-65455290 | Rare:81 | ||||
chr11:68338199-68338237 | Rare:4 | ||||
chr11:72018447-72018747 | Common:2; Rare:74 | ||||
chr11:73182853-73183185 | Common:1; Rare:61 | ||||
chr11:73309256-73309504 | Common:1; Rare:92 |