Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:234373331-234373578 | Common:1; Rare:121; Clinvar (benign):4 | ||||
chr1:236523879-236524010 | Common:2; Rare:33 | ||||
chr1:243255783-243256071 | Rare:78; Clinvar:3 | ||||
chr10:1048873-1049101 | Common:2; Rare:116 | ||||
chr10:7787975-7788222 | Common:1; Rare:98 | ||||
chr10:12195790-12196238 | Rare:119 | ||||
chr10:14878657-14878884 | Common:2; Rare:64 | ||||
chr10:27155197-27155397 | Common:4; Rare:76; Clinvar:3; Clinvar (benign):4 | ||||
chr10:31319022-31319222 | Common:2; Rare:60 | ||||
chr10:32958153-32958415 | Common:2; Rare:100 | ||||
chr10:43407770-43407874 | Common:1; Rare:44 | ||||
chr10:45972387-45972577 | Rare:60 | ||||
chr10:49941947-49942091 | Rare:35 | ||||
chr10:68331907-68332105 | Common:1; Rare:86 | ||||
chr10:73167958-73168137 | Rare:42 |