Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43358672-43359004 | Common:7; Rare:102 | ||||
chr1:43367950-43368208 | Rare:67 | ||||
chr1:43389757-43389940 | Common:3; Rare:81 | ||||
chr1:43946626-43946987 | Rare:97 | ||||
chr1:44674425-44674760 | Common:3; Rare:85 | ||||
chr1:44775469-44775607 | Rare:55 | ||||
chr1:44808393-44808561 | Common:1; Rare:40 | ||||
chr1:45500081-45500351 | Common:1; Rare:69; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521849-45522069 | Common:1; Rare:88 | ||||
chr1:45687059-45687353 | Common:1; Rare:77 | ||||
chr1:45688079-45688237 | Common:1; Rare:48 | ||||
chr1:45750618-45750839 | Rare:81 | ||||
chr1:46303138-46303294 | Common:1; Rare:51 | ||||
chr1:46303310-46303775 | Common:2; Rare:127 | ||||
chr1:51878689-51879009 | Common:1; Rare:91 |