Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:3575107-3575447 | Common:2; Rare:98; Clinvar:3; Clinvar (benign):6 | ||||
chr2:9003955-9004074 | Rare:43 | ||||
chr2:9423127-9423676 | Common:1; Rare:144 | ||||
chr2:9474475-9474569 | Common:7; Rare:42 | ||||
chr2:9555719-9555943 | Common:2; Rare:76 | ||||
chr2:9843204-9843508 | Common:7; Rare:88 | ||||
chr2:9843645-9843721 | Common:2; Rare:29 | ||||
chr2:12716756-12717047 | Common:1; Rare:86 | ||||
chr2:17540456-17540714 | Common:1; Rare:61 | ||||
chr2:17753769-17753876 | Common:1; Rare:41 | ||||
chr2:19990079-19990211 | Rare:34 | ||||
chr2:20225061-20225153 | Common:1; Rare:30 | ||||
chr2:20225365-20225603 | Common:1; Rare:59 | ||||
chr2:20350805-20351071 | Common:1; Rare:114 | ||||
chr2:20446877-20447113 | Common:3; Rare:96 |