Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43707352-43707566 | Common:2; Rare:60 | ||||
chr1:43946607-43946930 | Rare:82 | ||||
chr1:44674433-44674734 | Common:3; Rare:73 | ||||
chr1:44777609-44778040 | Common:2; Rare:108 | ||||
chr1:45339996-45340171 | Rare:52 | ||||
chr1:45500102-45500358 | Rare:61; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521880-45522018 | Common:1; Rare:52 | ||||
chr1:45583940-45584198 | Common:1; Rare:96 | ||||
chr1:45688050-45688253 | Common:1; Rare:56 | ||||
chr1:45750585-45750839 | Rare:92 | ||||
chr1:46132623-46132736 | Rare:45 | ||||
chr1:46198338-46198517 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
chr1:46303596-46303733 | Common:1; Rare:37 | ||||
chr1:46340606-46340777 | Common:2; Rare:41 | ||||
chr1:51236193-51236392 | Common:2; Rare:77 |