Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:27504066-27504372 | Rare:144; Clinvar:4; Clinvar (benign):1 | ||||
chr10:28532430-28532862 | Common:5; Rare:163 | ||||
chr10:29522728-29523038 | Common:2; Rare:55 | ||||
chr10:29735775-29735949 | Common:3; Rare:31 | ||||
chr10:30059501-30059617 | Common:1; Rare:45 | ||||
chr10:30434555-30434657 | Rare:32 | ||||
chr10:31031846-31032046 | Common:2; Rare:79 | ||||
chr10:31319006-31319244 | Common:2; Rare:70 | ||||
chr10:31320891-31321253 | Rare:89 | ||||
chr10:31928729-31928926 | Common:3; Rare:77 | ||||
chr10:32055969-32056226 | Common:1; Rare:96 | ||||
chr10:32378684-32378878 | Rare:24 | ||||
chr10:32446068-32446301 | Common:1; Rare:104 | ||||
chr10:32958149-32958478 | Common:2; Rare:126 | ||||
chr10:33335206-33335286 | Rare:18 |