Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43946571-43946983 | Rare:108 | ||||
chr1:43974778-43975035 | Common:3; Rare:69 | ||||
chr1:44213382-44213498 | Common:1; Rare:24 | ||||
chr1:44674425-44674722 | Common:3; Rare:76 | ||||
chr1:44775462-44775607 | Rare:55 | ||||
chr1:44777612-44778067 | Common:2; Rare:113 | ||||
chr1:45339996-45340046 | Rare:14 | ||||
chr1:45340103-45340178 | Rare:28 | ||||
chr1:45340388-45340496 | Common:1; Rare:28; Clinvar:1 | ||||
chr1:45500056-45500385 | Common:1; Rare:92; Clinvar:5; Clinvar (pathogenic):3 | ||||
chr1:45521811-45521999 | Common:1; Rare:74 | ||||
chr1:45583970-45584101 | Rare:52 | ||||
chr1:45687050-45687353 | Common:1; Rare:81 | ||||
chr1:45688055-45688250 | Common:1; Rare:56 | ||||
chr1:45913492-45913667 | Rare:30 |