Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44674421-44674724 | Common:3; Rare:79 | ||||
chr1:44739605-44739935 | Common:3; Rare:131 | ||||
chr1:44775438-44775607 | Common:1; Rare:66 | ||||
chr1:44775783-44776140 | Common:2; Rare:131 | ||||
chr1:44776574-44776773 | Rare:65 | ||||
chr1:44986552-44986791 | Common:2; Rare:46; Clinvar (benign):1 | ||||
chr1:45012031-45012283 | Common:1; Rare:87; Clinvar:4; Clinvar (benign):1 | ||||
chr1:45326755-45326912 | Rare:39 | ||||
chr1:45339949-45340206 | Common:1; Rare:96; Clinvar (benign):2 | ||||
chr1:45340381-45340470 | Common:1; Rare:24; Clinvar:1 | ||||
chr1:45491149-45491403 | Common:2; Rare:67 | ||||
chr1:45499954-45500373 | Common:2; Rare:100; Clinvar:5; Clinvar (pathogenic):3 | ||||
chr1:45521827-45522089 | Common:1; Rare:101 | ||||
chr1:45550706-45551071 | Common:3; Rare:93 | ||||
chr1:45583931-45584066 | Rare:51 |