Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:40134581-40135035 | Rare:141; Clinvar:1 | ||||
chr7:42932163-42932410 | Rare:100 | ||||
chr7:43926341-43926495 | Rare:48 | ||||
chr7:44044617-44044740 | Common:1; Rare:32 | ||||
chr7:44104626-44104668 | Rare:17 | ||||
chr7:44490608-44490733 | Rare:45 | ||||
chr7:44573899-44574077 | Common:3; Rare:53 | ||||
chr7:44606433-44606653 | Common:1; Rare:73 | ||||
chr7:44748343-44748591 | Common:2; Rare:61 | ||||
chr7:44796395-44796787 | Common:3; Rare:150 | ||||
chr7:45111665-45111799 | Common:1; Rare:50 | ||||
chr7:50450322-50450445 | Common:1; Rare:50 | ||||
chr7:55572341-55572591 | Common:1; Rare:100 | ||||
chr7:56051439-56051863 | Common:1; Rare:164; Clinvar:5; Clinvar (benign):1 | ||||
chr7:56106418-56106710 | Common:8; Rare:98 |