Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:208025480-208025629 | Common:1; Rare:38 | ||||
chr2:208254384-208254595 | Common:1; Rare:44 | ||||
chr2:208255005-208255234 | Common:2; Rare:59 | ||||
chr2:208266121-208266306 | Common:6; Rare:65; Clinvar:1; Clinvar (benign):2 | ||||
chr2:210477580-210477696 | Rare:40 | ||||
chr2:212538576-212538893 | Common:1; Rare:98 | ||||
chr2:212539138-212539455 | Common:6; Rare:59 | ||||
chr2:213284210-213284521 | Rare:105 | ||||
chr2:214809609-214809991 | Common:4; Rare:137; Clinvar:1; Clinvar (benign):3 | ||||
chr2:215311879-215312139 | Common:8; Rare:100 | ||||
chr2:215435849-215435905 | Rare:8 | ||||
chr2:215436004-215436460 | Common:2; Rare:124 | ||||
chr2:216081761-216081882 | Rare:35 | ||||
chr2:216498740-216498894 | Common:6; Rare:65 | ||||
chr2:216694438-216694858 | Rare:102 |