Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:208255019-208255238 | Common:2; Rare:58 | ||||
chr2:208266070-208266286 | Common:7; Rare:70; Clinvar:1; Clinvar (benign):2 | ||||
chr2:210477582-210477699 | Rare:39 | ||||
chr2:213284243-213284483 | Rare:77 | ||||
chr2:215311871-215312139 | Common:8; Rare:102 | ||||
chr2:215435996-215436253 | Common:2; Rare:80 | ||||
chr2:216081782-216081906 | Common:1; Rare:39 | ||||
chr2:216498721-216498886 | Common:6; Rare:67 | ||||
chr2:218217105-218217226 | Rare:50 | ||||
chr2:218270082-218270538 | Common:5; Rare:144; Clinvar:3; Clinvar (benign):1 | ||||
chr2:218287223-218287427 | Common:1; Rare:35 | ||||
chr2:218568293-218568933 | Common:5; Rare:165 | ||||
chr2:218659603-218659738 | Rare:32 | ||||
chr2:218671963-218672061 | Rare:33 | ||||
chr2:219176907-219177046 | Common:3; Rare:40 |