Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42658286-42658436 | Common:2; Rare:41 | ||||
chr1:42767003-42767292 | Common:4; Rare:91; Clinvar (benign):1 | ||||
chr1:42846392-42846635 | Common:1; Rare:67 | ||||
chr1:42958821-42959007 | Common:2; Rare:47; Clinvar:3; Clinvar (benign):3 | ||||
chr1:43358674-43359030 | Common:7; Rare:112 | ||||
chr1:43367989-43368130 | Rare:35 | ||||
chr1:43389768-43389909 | Common:3; Rare:53 | ||||
chr1:45339978-45340212 | Rare:83; Clinvar:1; Clinvar (benign):3 | ||||
chr1:45521873-45522072 | Common:1; Rare:77 | ||||
chr1:45687059-45687353 | Common:1; Rare:77 | ||||
chr1:46303162-46303288 | Common:1; Rare:44 | ||||
chr1:46303318-46303747 | Common:2; Rare:114 | ||||
chr1:52055158-52055252 | Common:1; Rare:22 | ||||
chr1:52056078-52056337 | Common:2; Rare:74 | ||||
chr1:52404467-52404618 | Common:1; Rare:45 |