Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:78168517-78168634 | Rare:38 | ||||
chr17:78187045-78187386 | Common:3; Rare:109 | ||||
chr17:78378589-78378719 | Common:1; Rare:55 | ||||
chr17:78782218-78782564 | Common:9; Rare:113 | ||||
chr17:78840736-78841060 | Common:2; Rare:118 | ||||
chr17:79022728-79022976 | Common:2; Rare:52 | ||||
chr17:79023339-79023445 | Rare:27 | ||||
chr17:79024004-79024318 | Common:3; Rare:70 | ||||
chr17:79024732-79025096 | Common:4; Rare:71 | ||||
chr17:80035840-80036031 | Common:1; Rare:66 | ||||
chr17:80147109-80147360 | Common:5; Rare:98 | ||||
chr17:80220309-80220468 | Common:1; Rare:61; Clinvar:1; Clinvar (pathogenic):2 | ||||
chr17:80414867-80415189 | Common:3; Rare:159 | ||||
chr17:81511902-81512424 | Common:3; Rare:253; Clinvar:8; Clinvar (benign):31; Clinvar (pathogenic):2 | ||||
chr17:81566508-81566649 | Common:1; Rare:34 |