Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:6612109-6612513 | Common:4; Rare:128 | ||||
chr11:6612523-6612841 | Common:3; Rare:67; Clinvar:2 | ||||
chr11:6619326-6619597 | Common:3; Rare:87; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr11:6683013-6683114 | Rare:30 | ||||
chr11:6683233-6683734 | Common:6; Rare:181 | ||||
chr11:6926253-6926630 | Common:5; Rare:112 | ||||
chr11:6926829-6926974 | Common:1; Rare:28 | ||||
chr11:7020274-7020531 | Rare:85 | ||||
chr11:7512514-7512972 | Rare:65 | ||||
chr11:7513267-7513423 | Rare:22 | ||||
chr11:7513552-7514160 | Common:8; Rare:174 | ||||
chr11:7673435-7673623 | Common:1; Rare:63 | ||||
chr11:7674236-7674338 | Rare:41 | ||||
chr11:7986993-7987408 | Common:10; Rare:158 | ||||
chr11:8168512-8168629 | Common:2; Rare:33 |