Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:188292753-188292869 | Common:1; Rare:30 | ||||
chr2:188974500-188974571 | Rare:20; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr2:189179580-189179880 | Common:1; Rare:52; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr2:189441086-189441507 | Common:2; Rare:126 | ||||
chr2:189783958-189784096 | Common:3; Rare:46; Clinvar (benign):1 | ||||
chr2:189784264-189784564 | Common:4; Rare:107; Clinvar:8; Clinvar (benign):3 | ||||
chr2:190343883-190344029 | Rare:27 | ||||
chr2:190534688-190534805 | Common:1; Rare:37 | ||||
chr2:190648700-190648937 | Common:1; Rare:85 | ||||
chr2:191245231-191245615 | Common:4; Rare:121 | ||||
chr2:191246155-191246326 | Common:1; Rare:48 | ||||
chr2:197453244-197453552 | Rare:102 | ||||
chr2:197499803-197500191 | Rare:135; Clinvar:1; Clinvar (benign):1 | ||||
chr2:197500201-197500435 | Common:1; Rare:98 | ||||
chr2:200306432-200306745 | Common:3; Rare:88 |