Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:61816120-61816359 | Rare:65 | ||||
chr11:61967449-61967488 | Rare:14 | ||||
chr11:61967562-61967816 | Common:4; Rare:95; Clinvar:3 | ||||
chr11:62545604-62545952 | Common:1; Rare:77 | ||||
chr11:62612564-62612651 | Common:1; Rare:22 | ||||
chr11:62626608-62626914 | Common:2; Rare:82 | ||||
chr11:62646560-62646777 | Common:1; Rare:89; Clinvar (pathogenic):1 | ||||
chr11:62653289-62653412 | Common:1; Rare:32 | ||||
chr11:62665133-62665327 | Common:4; Rare:89 | ||||
chr11:62678907-62679174 | Rare:87 | ||||
chr11:62706216-62706426 | Common:3; Rare:89; Clinvar (benign):5 | ||||
chr11:62709501-62709724 | Common:1; Rare:93 | ||||
chr11:62727390-62727697 | Rare:131 | ||||
chr11:62728418-62728531 | Common:1; Rare:68 | ||||
chr11:62754126-62754263 | Common:1; Rare:38 |