Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:25673389-25673761 | Common:1; Rare:132 | ||||
chr2:25878442-25878645 | Common:1; Rare:60 | ||||
chr2:25982518-25982818 | Common:1; Rare:72 | ||||
chr2:26033751-26034193 | Common:4; Rare:167 | ||||
chr2:26244573-26244989 | Common:2; Rare:154; Clinvar:6; Clinvar (benign):9 | ||||
chr2:26319060-26319111 | Rare:14 | ||||
chr2:26345750-26346187 | Common:2; Rare:131 | ||||
chr2:26764173-26764337 | Common:1; Rare:67 | ||||
chr2:26785724-26786107 | Rare:102 | ||||
chr2:27032844-27033015 | Rare:66 | ||||
chr2:27051539-27051786 | Rare:74 | ||||
chr2:27071595-27071872 | Common:1; Rare:84 | ||||
chr2:27086593-27086855 | Common:3; Rare:72; Clinvar (benign):3 | ||||
chr2:27086988-27087249 | Common:1; Rare:53; Clinvar:3 | ||||
chr2:27134606-27134749 | Rare:61 |