Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:207322110-207322390 | Rare:80 | ||||
chr1:207496057-207496271 | Rare:43 | ||||
chr1:207751856-207752309 | Common:2; Rare:157; Clinvar:1 | ||||
chr1:208244205-208244502 | Common:2; Rare:82 | ||||
chr1:209652384-209652614 | Common:3; Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
chr1:209675259-209675861 | Common:4; Rare:161 | ||||
chr1:209806002-209806269 | Common:4; Rare:68; Clinvar:2; Clinvar (benign):2 | ||||
chr1:209827838-209828111 | Common:1; Rare:74 | ||||
chr1:211259073-211259404 | Common:1; Rare:106 | ||||
chr1:211675546-211675787 | Common:1; Rare:50 | ||||
chr1:212035489-212035801 | Common:2; Rare:88 | ||||
chr1:212285072-212285418 | Common:3; Rare:115 | ||||
chr1:212432798-212433114 | Rare:84 | ||||
chr1:212791746-212791964 | Common:5; Rare:101 | ||||
chr1:212858089-212858303 | Common:4; Rare:55; Clinvar:2 |