Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155210362-155210629 | Rare:89 | ||||
chr1:155255373-155255503 | Common:1; Rare:27 | ||||
chr1:155262089-155262451 | Common:3; Rare:110 | ||||
chr1:155308576-155309019 | Common:1; Rare:96 | ||||
chr1:155317708-155318019 | Common:1; Rare:55; Clinvar (pathogenic):1 | ||||
chr1:155320648-155320878 | Common:1; Rare:75 | ||||
chr1:155324155-155324616 | Common:3; Rare:163 | ||||
chr1:155349583-155349699 | Rare:23 | ||||
chr1:155562679-155563042 | Common:1; Rare:189 | ||||
chr1:155563096-155563268 | Rare:72 | ||||
chr1:155612660-155612841 | Rare:36 | ||||
chr1:155688596-155688817 | Common:1; Rare:59 | ||||
chr1:155727391-155727581 | Common:1; Rare:37 | ||||
chr1:155729049-155729367 | Common:1; Rare:89 | ||||
chr1:155859328-155859533 | Common:2; Rare:49 |