Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179882418-179882728 | Rare:133; Clinvar:2; Clinvar (benign):2 | ||||
chr1:182789641-182789798 | Common:2; Rare:56 | ||||
chr1:182839200-182839371 | Common:1; Rare:72 | ||||
chr1:183635637-183636100 | Common:4; Rare:130 | ||||
chr1:184386840-184387300 | Common:1; Rare:108 | ||||
chr1:184387302-184387348 | Rare:10 | ||||
chr1:185156885-185157297 | Common:2; Rare:116 | ||||
chr1:186375200-186375471 | Rare:63 | ||||
chr1:186375709-186375937 | Common:1; Rare:61 | ||||
chr1:193059236-193059673 | Rare:202 | ||||
chr1:193122078-193122194 | Common:1; Rare:38; Clinvar:2; Clinvar (benign):3 | ||||
chr1:201955253-201955525 | Common:1; Rare:76 | ||||
chr1:202927121-202927376 | Common:5; Rare:116 | ||||
chr1:203007263-203007451 | Common:2; Rare:75 | ||||
chr1:204516243-204516498 | Common:1; Rare:78 |