Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42817009-42817136 | Common:1; Rare:32 | ||||
chr1:42817214-42817351 | Rare:60 | ||||
chr1:42846405-42846635 | Common:1; Rare:61 | ||||
chr1:42958754-42959084 | Common:4; Rare:86; Clinvar:6; Clinvar (benign):4 | ||||
chr1:43358666-43359006 | Common:7; Rare:107 | ||||
chr1:43367914-43368190 | Rare:70 | ||||
chr1:43389757-43389971 | Common:4; Rare:93; Clinvar:1 | ||||
chr1:43946561-43946983 | Rare:113 | ||||
chr1:43969784-43970011 | Rare:55 | ||||
chr1:44213348-44213498 | Common:1; Rare:28 | ||||
chr1:44674425-44674717 | Common:3; Rare:76 | ||||
chr1:44775487-44775599 | Rare:48 | ||||
chr1:44777611-44778116 | Common:2; Rare:126 | ||||
chr1:45340408-45340488 | Common:1; Rare:21; Clinvar:1 | ||||
chr1:45550580-45550894 | Common:2; Rare:76 |