Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11273409-11273523 | Common:1; Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
chr1:11654417-11654511 | Rare:26 | ||||
chr1:11654826-11654925 | Common:1; Rare:24 | ||||
chr1:11735779-11736082 | Common:1; Rare:66 | ||||
chr1:11805476-11805658 | Common:2; Rare:35 | ||||
chr1:11805900-11806265 | Common:2; Rare:100; Clinvar:1 | ||||
chr1:11980069-11980374 | Common:4; Rare:93; Clinvar:1; Clinvar (benign):2 | ||||
chr1:11980406-11980504 | Common:1; Rare:32; Clinvar (benign):3 | ||||
chr1:12019242-12019539 | Common:5; Rare:103 | ||||
chr1:12192142-12192444 | Rare:86 | ||||
chr1:12344566-12344908 | Rare:54 | ||||
chr1:12496558-12496849 | Common:3; Rare:56 | ||||
chr1:12496866-12497047 | Common:1; Rare:32 | ||||
chr1:12596308-12596554 | Rare:61 | ||||
chr1:12617163-12617440 | Rare:84 |