Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:173867981-173868203 | Common:1; Rare:76 | ||||
chr1:174999648-175000164 | Common:3; Rare:169 | ||||
chr1:179882199-179882820 | Rare:219; Clinvar:7; Clinvar (benign):2 | ||||
chr1:182391334-182391438 | Rare:23 | ||||
chr1:182839194-182839376 | Common:1; Rare:78 | ||||
chr1:183635777-183636089 | Common:2; Rare:80 | ||||
chr1:183805049-183805168 | Rare:32 | ||||
chr1:184051651-184051753 | Common:2; Rare:37 | ||||
chr1:184754650-184754917 | Common:1; Rare:75 | ||||
chr1:185156941-185157291 | Common:1; Rare:94 | ||||
chr1:185317197-185317468 | Common:1; Rare:80 | ||||
chr1:186375123-186375520 | Rare:105 | ||||
chr1:186375667-186375899 | Common:1; Rare:61 | ||||
chr1:192808805-192809070 | Common:4; Rare:112 | ||||
chr1:193059330-193059659 | Rare:152 |