Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:3377791-3377984 | Rare:54 | ||||
chr2:3379633-3379779 | Common:2; Rare:61 | ||||
chr2:3558269-3558484 | Common:5; Rare:90 | ||||
chr2:3575098-3575345 | Common:2; Rare:69; Clinvar:2; Clinvar (benign):5 | ||||
chr2:9423402-9423714 | Rare:99 | ||||
chr2:9474350-9474630 | Common:8; Rare:93 | ||||
chr2:9555678-9555918 | Common:2; Rare:77 | ||||
chr2:9630944-9631286 | Common:2; Rare:107 | ||||
chr2:9843251-9843501 | Common:6; Rare:69 | ||||
chr2:10689906-10690018 | Common:2; Rare:40 | ||||
chr2:10812704-10812996 | Common:3; Rare:110 | ||||
chr2:11132771-11132810 | Rare:7 | ||||
chr2:12716795-12717053 | Common:1; Rare:77 | ||||
chr2:15561298-15561392 | Rare:41 | ||||
chr2:15940353-15940576 | Rare:53 |