Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:58347591-58347751 | Common:7; Rare:79 | ||||
chr19:58408452-58408686 | Common:3; Rare:71 | ||||
chr19:58499230-58499538 | Common:1; Rare:94; Clinvar:1 | ||||
chr19:58554903-58555255 | Common:2; Rare:120 | ||||
chr2:677346-677525 | Common:1; Rare:73 | ||||
chr2:3377817-3377964 | Rare:40 | ||||
chr2:3379608-3379766 | Common:1; Rare:65 | ||||
chr2:3519506-3519660 | Common:1; Rare:38 | ||||
chr2:3558269-3558565 | Common:6; Rare:108 | ||||
chr2:3575107-3575447 | Common:2; Rare:98; Clinvar:3; Clinvar (benign):6 | ||||
chr2:9423168-9423289 | Common:1; Rare:27 | ||||
chr2:9423439-9423697 | Rare:84 | ||||
chr2:9474508-9474575 | Common:6; Rare:41 | ||||
chr2:9555730-9556057 | Common:2; Rare:108 | ||||
chr2:9630944-9631316 | Common:3; Rare:119 |