Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:208255014-208255232 | Common:2; Rare:56 | ||||
chr2:208266032-208266276 | Common:9; Rare:86; Clinvar:1; Clinvar (benign):2 | ||||
chr2:210002514-210002663 | Common:4; Rare:55 | ||||
chr2:210477580-210477685 | Rare:35 | ||||
chr2:213284210-213284483 | Rare:88 | ||||
chr2:215375208-215375725 | Common:2; Rare:139 | ||||
chr2:215409550-215410140 | Rare:156 | ||||
chr2:215435309-215435616 | Common:1; Rare:83 | ||||
chr2:215435643-215436140 | Common:3; Rare:123 | ||||
chr2:216081777-216081889 | Rare:36 | ||||
chr2:216498754-216498893 | Common:4; Rare:60 | ||||
chr2:218217057-218217246 | Common:1; Rare:67 | ||||
chr2:218568307-218568592 | Common:2; Rare:74 | ||||
chr2:218659600-218659733 | Rare:32 | ||||
chr2:218671967-218672062 | Rare:33 |