Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:44112001-44112233 | Common:1; Rare:70 | ||||
chr7:44123509-44123733 | Common:3; Rare:61 | ||||
chr7:44573888-44574068 | Common:3; Rare:54 | ||||
chr7:44582169-44582525 | Common:1; Rare:135 | ||||
chr7:44606465-44606631 | Common:1; Rare:59 | ||||
chr7:44796395-44796791 | Common:3; Rare:151 | ||||
chr7:45111672-45111799 | Common:1; Rare:48 | ||||
chr7:47582573-47582738 | Rare:42 | ||||
chr7:47979507-47979742 | Rare:87 | ||||
chr7:50450329-50450438 | Rare:44 | ||||
chr7:55019026-55019295 | Common:2; Rare:79; Clinvar:3; Clinvar (benign):2 | ||||
chr7:55365933-55366069 | Rare:59 | ||||
chr7:56051416-56051840 | Common:1; Rare:161; Clinvar:5; Clinvar (benign):1 | ||||
chr7:56064185-56064367 | Common:2; Rare:112 | ||||
chr7:65982179-65982342 | Common:2; Rare:49; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 |