Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:25251122-25251299 | Common:2; Rare:27 | ||||
chr2:25277333-25277472 | Common:1; Rare:40 | ||||
chr2:25540516-25540561 | Rare:10 | ||||
chr2:26052494-26052653 | Rare:24 | ||||
chr2:26193757-26193878 | Rare:38; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr2:27226796-27226882 | Rare:26 | ||||
chr2:27265117-27265240 | Rare:20 | ||||
chr2:27351865-27352116 | Common:1; Rare:55 | ||||
chr2:27382125-27382608 | Rare:85 | ||||
chr2:27437066-27437226 | Common:1; Rare:28 | ||||
chr2:27715706-27715938 | Common:1; Rare:38 | ||||
chr2:27716026-27716145 | Rare:7 | ||||
chr2:27752668-27752905 | Rare:36 | ||||
chr2:32358030-32358150 | Common:2; Rare:20 | ||||
chr2:32817192-32817498 | Common:1; Rare:76 |