Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45340386-45340488 | Common:1; Rare:27; Clinvar:1 | ||||
chr1:45500050-45500385 | Common:1; Rare:93; Clinvar:5; Clinvar (pathogenic):3 | ||||
chr1:45521647-45522135 | Common:1; Rare:170 | ||||
chr1:45522777-45522933 | Rare:27 | ||||
chr1:45522951-45523040 | Common:1; Rare:14 | ||||
chr1:45550715-45551107 | Common:3; Rare:95 | ||||
chr1:45583931-45584220 | Common:1; Rare:110 | ||||
chr1:45686479-45686677 | Rare:74 | ||||
chr1:45687017-45687357 | Common:2; Rare:89 | ||||
chr1:45688049-45688243 | Common:1; Rare:54 | ||||
chr1:45750606-45750856 | Rare:89 | ||||
chr1:46132626-46132755 | Rare:46 | ||||
chr1:46198358-46198537 | Common:1; Rare:73; Clinvar:1 | ||||
chr1:46247372-46247714 | Common:4; Rare:65 | ||||
chr1:46303135-46303820 | Common:3; Rare:203 |