Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40818720-40818977 | Common:6; Rare:52 | ||||
chr1:40979583-40979809 | Common:3; Rare:81 | ||||
chr1:42335099-42335395 | Common:6; Rare:143 | ||||
chr1:42455993-42456107 | Rare:40 | ||||
chr1:42456446-42456586 | Rare:62 | ||||
chr1:42658093-42658515 | Common:3; Rare:111 | ||||
chr1:42682154-42682500 | Common:2; Rare:98 | ||||
chr1:42740225-42740446 | Common:1; Rare:48 | ||||
chr1:42766976-42767327 | Common:6; Rare:122; Clinvar (benign):1 | ||||
chr1:42816635-42816692 | Rare:12 | ||||
chr1:42817030-42817136 | Common:1; Rare:25 | ||||
chr1:42817169-42817548 | Rare:121 | ||||
chr1:42846381-42846656 | Common:1; Rare:81 | ||||
chr1:42958714-42959104 | Common:4; Rare:96; Clinvar:6; Clinvar (benign):4 | ||||
chr1:43172193-43172359 | Common:1; Rare:71 |