Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:206159396-206159683 | Common:2; Rare:95 | ||||
chr2:206765297-206765623 | Common:2; Rare:79; Clinvar:4; Clinvar (benign):1 | ||||
chr2:207625226-207625591 | Common:1; Rare:101 | ||||
chr2:208255064-208255228 | Common:2; Rare:44 | ||||
chr2:210477568-210477685 | Rare:36 | ||||
chr2:215311871-215312091 | Common:5; Rare:80 | ||||
chr2:216498740-216498887 | Common:5; Rare:60 | ||||
chr2:218217064-218217206 | Common:1; Rare:52 | ||||
chr2:218270099-218270568 | Common:5; Rare:146; Clinvar:4; Clinvar (benign):2 | ||||
chr2:218659586-218659730 | Rare:32 | ||||
chr2:218671967-218672339 | Common:2; Rare:93 | ||||
chr2:219176926-219177046 | Common:3; Rare:35 | ||||
chr2:219178142-219178470 | Common:6; Rare:135 | ||||
chr2:219206628-219206925 | Rare:111 | ||||
chr2:219229584-219229891 | Common:1; Rare:90 |