Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:63593337-63593447 | Rare:41; Clinvar (benign):1 | ||||
chr1:66924845-66925046 | Rare:81 | ||||
chr1:66925187-66925355 | Common:2; Rare:53 | ||||
chr1:66930083-66930385 | Rare:99 | ||||
chr1:67053943-67054137 | Common:1; Rare:78 | ||||
chr1:67429991-67430226 | Rare:83 | ||||
chr1:67430235-67430582 | Rare:129 | ||||
chr1:68497031-68497207 | Common:2; Rare:61 | ||||
chr1:70205542-70205770 | Rare:72 | ||||
chr1:70221283-70221506 | Rare:94 | ||||
chr1:70354699-70354856 | Rare:55 | ||||
chr1:70411069-70411291 | Common:2; Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080997-71081393 | Rare:107 | ||||
chr1:74198091-74198351 | Common:3; Rare:136 | ||||
chr1:74733030-74733269 | Common:5; Rare:77 |