Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:206159405-206159672 | Common:1; Rare:89 | ||||
chr2:206765324-206765615 | Common:2; Rare:69; Clinvar:3; Clinvar (benign):1 | ||||
chr2:207625312-207625591 | Common:1; Rare:81 | ||||
chr2:208255032-208255221 | Common:2; Rare:49 | ||||
chr2:208266074-208266246 | Common:4; Rare:52 | ||||
chr2:210477568-210477624 | Rare:21 | ||||
chr2:215311879-215312076 | Common:3; Rare:68 | ||||
chr2:215436037-215436307 | Common:2; Rare:90 | ||||
chr2:216081782-216081889 | Rare:33 | ||||
chr2:216498740-216498875 | Common:5; Rare:53 | ||||
chr2:218270106-218270532 | Common:5; Rare:128; Clinvar:2; Clinvar (benign):1 | ||||
chr2:218659621-218659740 | Rare:28 | ||||
chr2:218671977-218672060 | Rare:29 | ||||
chr2:219176926-219177109 | Common:4; Rare:57 | ||||
chr2:219229340-219229436 | Rare:27 |