Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:41703037-41703268 | Common:2; Rare:33 | ||||
chr7:42932164-42932395 | Rare:89 | ||||
chr7:43869477-43869663 | Rare:58 | ||||
chr7:43926368-43926445 | Rare:27 | ||||
chr7:44104610-44104896 | Common:1; Rare:92 | ||||
chr7:44123523-44123852 | Common:4; Rare:98 | ||||
chr7:44490589-44490723 | Common:1; Rare:53 | ||||
chr7:44573899-44574069 | Common:3; Rare:48 | ||||
chr7:44582169-44582529 | Common:1; Rare:136 | ||||
chr7:44748319-44748585 | Common:2; Rare:66 | ||||
chr7:44796397-44796725 | Common:3; Rare:134 | ||||
chr7:45111676-45111799 | Common:1; Rare:46 | ||||
chr7:50450329-50450441 | Rare:45 | ||||
chr7:56051439-56051845 | Common:1; Rare:156; Clinvar:5; Clinvar (benign):1 | ||||
chr7:56106419-56106710 | Common:8; Rare:98 |