Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:4393651-4393814 | Rare:41 | ||||
chr11:5624881-5625029 | Rare:25 | ||||
chr11:6390221-6390522 | Common:2; Rare:91 | ||||
chr11:6419058-6419150 | Common:2; Rare:20 | ||||
chr11:6473703-6474113 | Rare:101 | ||||
chr11:6481276-6481569 | Common:5; Rare:131 | ||||
chr11:6603542-6603822 | Common:4; Rare:86; Clinvar (benign):3 | ||||
chr11:6604671-6604829 | Common:3; Rare:40 | ||||
chr11:6612661-6612735 | Common:1; Rare:12 | ||||
chr11:6683234-6683650 | Common:6; Rare:158 | ||||
chr11:6926389-6926442 | Common:4; Rare:12 | ||||
chr11:6926837-6926992 | Common:1; Rare:33 | ||||
chr11:7020316-7020458 | Rare:47 | ||||
chr11:7513604-7513996 | Common:6; Rare:121 | ||||
chr11:7573758-7573989 | Rare:47 |