Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44777524-44777665 | Common:1; Rare:32 | ||||
chr1:44777700-44777997 | Common:1; Rare:89 | ||||
chr1:44799603-44799957 | Common:2; Rare:67 | ||||
chr1:44800164-44800393 | Common:1; Rare:51 | ||||
chr1:44800668-44800853 | Rare:56 | ||||
chr1:44801550-44801816 | Common:1; Rare:90 | ||||
chr1:44808160-44808668 | Common:3; Rare:107 | ||||
chr1:44808847-44808913 | Rare:19 | ||||
chr1:44810906-44811213 | Common:1; Rare:39 | ||||
chr1:44811259-44811652 | Common:2; Rare:76 | ||||
chr1:44811696-44811771 | Rare:13 | ||||
chr1:44986490-44986791 | Common:3; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
chr1:45006767-45006954 | Rare:43 | ||||
chr1:45008344-45008550 | Common:2; Rare:63 | ||||
chr1:45008662-45008753 | Rare:30 |