Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:88016545-88016802 | Common:7; Rare:107 | ||||
chr2:95525735-95525901 | Common:1; Rare:24 | ||||
chr2:95526712-95526847 | Common:1; Rare:48 | ||||
chr2:131682408-131682527 | Common:2; Rare:35 | ||||
chr2:162071188-162071300 | Rare:26 | ||||
chr2:170770779-170771070 | Common:2; Rare:51 | ||||
chr2:176637577-176637759 | Common:3; Rare:64 | ||||
chr2:176637936-176638087 | Common:2; Rare:37 | ||||
chr2:178413660-178413986 | Common:1; Rare:100 | ||||
chr2:200604016-200604220 | Rare:50 | ||||
chr2:207239397-207239674 | Rare:43 | ||||
chr2:215413266-215413403 | Common:1; Rare:22 | ||||
chr2:219420648-219420932 | Rare:77; Clinvar:7; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
chr2:226796073-226796217 | Rare:49 | ||||
chr2:239275918-239276035 | Common:1; Rare:28 |