Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:208266032-208266302 | Common:9; Rare:97; Clinvar:1; Clinvar (benign):2 | ||||
chr2:209423774-209424125 | Common:1; Rare:106 | ||||
chr2:210002473-210002664 | Common:5; Rare:65 | ||||
chr2:210477582-210477696 | Rare:39 | ||||
chr2:213284218-213284485 | Rare:87 | ||||
chr2:215311888-215312144 | Common:8; Rare:101 | ||||
chr2:215409562-215410115 | Rare:149 | ||||
chr2:215435656-215436253 | Common:4; Rare:162 | ||||
chr2:216081743-216081945 | Common:1; Rare:69 | ||||
chr2:216372139-216372219 | Rare:9 | ||||
chr2:216412714-216412775 | Rare:10 | ||||
chr2:216498689-216498909 | Common:7; Rare:96 | ||||
chr2:217978860-217978941 | Common:1; Rare:24 | ||||
chr2:218216966-218217246 | Common:2; Rare:98 | ||||
chr2:218270091-218270538 | Common:5; Rare:140; Clinvar:3; Clinvar (benign):1 |