Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45339949-45340243 | Common:1; Rare:110; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr1:45340386-45340579 | Common:1; Rare:47; Clinvar:1 | ||||
chr1:45499954-45500390 | Common:2; Rare:112; Clinvar:5; Clinvar (pathogenic):3 | ||||
chr1:45521827-45522083 | Common:1; Rare:101 | ||||
chr1:45550741-45551086 | Common:3; Rare:83 | ||||
chr1:45614776-45615068 | Common:1; Rare:69 | ||||
chr1:45687021-45687353 | Common:2; Rare:88 | ||||
chr1:45688055-45688243 | Common:1; Rare:54 | ||||
chr1:45750618-45750831 | Rare:78 | ||||
chr1:46194384-46194445 | Rare:19; Clinvar:1 | ||||
chr1:46198358-46198537 | Common:1; Rare:73; Clinvar:1 | ||||
chr1:46303213-46303790 | Common:2; Rare:181 | ||||
chr1:46340647-46340826 | Common:3; Rare:51 | ||||
chr1:46604199-46604443 | Common:1; Rare:64 | ||||
chr1:46940877-46941007 | Rare:29 |