Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:153963504-153963739 | Common:1; Rare:63 | ||||
chr1:153967306-153967566 | Common:1; Rare:55 | ||||
chr1:153967624-153967902 | Common:1; Rare:52 | ||||
chr1:153986207-153986463 | Rare:67 | ||||
chr1:153990555-153990852 | Common:2; Rare:118 | ||||
chr1:154172906-154173203 | Common:1; Rare:53; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr1:154182650-154182710 | Rare:17 | ||||
chr1:154182986-154183105 | Rare:28 | ||||
chr1:154183111-154183254 | Rare:56 | ||||
chr1:154219918-154220244 | Common:5; Rare:87 | ||||
chr1:154220507-154220995 | Common:1; Rare:164 | ||||
chr1:154221252-154221372 | Rare:30 | ||||
chr1:154272684-154272776 | Rare:31; Clinvar:2 | ||||
chr1:154558884-154559099 | Common:1; Rare:75 | ||||
chr1:154627899-154628039 | Common:2; Rare:73 |