Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:183038448-183038536 | Common:2; Rare:29 | ||||
chr2:183078680-183078862 | Rare:38 | ||||
chr2:186486018-186486455 | Common:3; Rare:128 | ||||
chr2:186589761-186590101 | Rare:97 | ||||
chr2:186694550-186694673 | Rare:21 | ||||
chr2:187565745-187565804 | Rare:17 | ||||
chr2:187565900-187566156 | Common:4; Rare:59 | ||||
chr2:188291453-188292113 | Common:8; Rare:178 | ||||
chr2:188292616-188292961 | Common:1; Rare:78 | ||||
chr2:188292985-188293083 | Rare:15 | ||||
chr2:189441053-189441552 | Common:3; Rare:171 | ||||
chr2:189661377-189661603 | Common:4; Rare:72 | ||||
chr2:189783921-189784140 | Common:5; Rare:75; Clinvar:1; Clinvar (benign):2 | ||||
chr2:189784236-189784797 | Common:9; Rare:179; Clinvar:8; Clinvar (benign):4 | ||||
chr2:190319719-190319938 | Common:4; Rare:79; Clinvar (benign):5 |