Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:197500260-197500424 | Common:1; Rare:68 | ||||
chr2:200889045-200889385 | Common:2; Rare:111 | ||||
chr2:201642637-201642757 | Rare:62 | ||||
chr2:202912147-202912275 | Common:1; Rare:47 | ||||
chr2:206159414-206159672 | Rare:85 | ||||
chr2:206765297-206765615 | Common:2; Rare:77; Clinvar:3; Clinvar (benign):1 | ||||
chr2:208255032-208255235 | Common:2; Rare:52 | ||||
chr2:210477576-210477624 | Rare:21 | ||||
chr2:213284210-213284483 | Rare:88 | ||||
chr2:215436053-215436241 | Common:2; Rare:66 | ||||
chr2:218270082-218270534 | Common:5; Rare:141; Clinvar:2; Clinvar (benign):1 | ||||
chr2:218659600-218659738 | Rare:33 | ||||
chr2:218671977-218672036 | Rare:22 | ||||
chr2:219229577-219229873 | Common:2; Rare:82 | ||||
chr2:219245407-219245531 | Rare:35 |