Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:114581574-114581871 | Common:1; Rare:126 | ||||
chr1:114669965-114670330 | Common:1; Rare:100 | ||||
chr1:114670476-114670713 | Rare:44 | ||||
chr1:114716703-114716902 | Common:1; Rare:87; Clinvar:5; Clinvar (benign):1 | ||||
chr1:114757252-114757748 | Common:1; Rare:118 | ||||
chr1:114757901-114758213 | Common:3; Rare:94 | ||||
chr1:114780357-114780486 | Rare:31 | ||||
chr1:114780510-114780882 | Common:2; Rare:133 | ||||
chr1:115089440-115089646 | Common:3; Rare:80 | ||||
chr1:115089911-115090114 | Common:3; Rare:45 | ||||
chr1:115641772-115642061 | Common:3; Rare:93; Clinvar:2; Clinvar (benign):2 | ||||
chr1:115642138-115642341 | Common:2; Rare:51 | ||||
chr1:115642626-115642723 | Common:1; Rare:21 | ||||
chr1:115671607-115671733 | Common:1; Rare:32 | ||||
chr1:116372403-116372551 | Common:1; Rare:22 |