Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:78079767-78079927 | Common:2; Rare:50 | ||||
chr11:78139590-78139809 | Common:3; Rare:88; Clinvar:2 | ||||
chr11:78188592-78188823 | Common:2; Rare:68 | ||||
chr11:83071797-83072088 | Common:4; Rare:80 | ||||
chr11:83193626-83193797 | Common:1; Rare:80 | ||||
chr11:85628326-85628606 | Common:7; Rare:86 | ||||
chr11:85647875-85648054 | Common:2; Rare:47; Clinvar:2; Clinvar (benign):2 | ||||
chr11:88337676-88337888 | Common:4; Rare:100; Clinvar:5; Clinvar (benign):3 | ||||
chr11:90223021-90223241 | Common:2; Rare:87 | ||||
chr11:93741477-93741690 | Common:5; Rare:80 | ||||
chr11:93784189-93784342 | Common:2; Rare:53 | ||||
chr11:94493802-94494003 | Common:3; Rare:58; Clinvar (benign):1 | ||||
chr11:94973542-94973707 | Rare:49 | ||||
chr11:95790373-95790580 | Common:1; Rare:79 | ||||
chr11:95924066-95924127 | Rare:22 |