Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:119366804-119367018 | Common:1; Rare:53 | ||||
chr2:127885954-127885974 | Rare:3 | ||||
chr2:130181550-130181760 | Common:2; Rare:96 | ||||
chr2:130182100-130182279 | Common:1; Rare:65 | ||||
chr2:134918708-134918849 | Rare:53 | ||||
chr2:148020705-148021046 | Common:1; Rare:68; Clinvar (benign):2 | ||||
chr2:162318650-162318804 | Rare:29 | ||||
chr2:171434014-171434234 | Common:1; Rare:56 | ||||
chr2:177392672-177392790 | Rare:30; Clinvar:1 | ||||
chr2:197500313-197500416 | Common:1; Rare:43 | ||||
chr2:200889134-200889451 | Common:3; Rare:103 | ||||
chr2:206159436-206159672 | Rare:79 | ||||
chr2:206765312-206765612 | Common:1; Rare:71; Clinvar:3 | ||||
chr2:216498689-216498862 | Common:4; Rare:65 | ||||
chr2:218659359-218659733 | Common:4; Rare:85 |