Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:62687735-62687935 | Rare:54 | ||||
chr1:62688310-62688540 | Rare:66 | ||||
chr1:62784069-62784191 | Rare:50 | ||||
chr1:63322139-63322576 | Common:3; Rare:131 | ||||
chr1:63367417-63367699 | Rare:86; Clinvar (benign):1 | ||||
chr1:63523132-63523579 | Common:3; Rare:126 | ||||
chr1:63593135-63593510 | Rare:128; Clinvar (benign):2 | ||||
chr1:63593621-63593720 | Rare:51; Clinvar (pathogenic):1 | ||||
chr1:63773880-63774439 | Common:2; Rare:120 | ||||
chr1:63775129-63775219 | Rare:33 | ||||
chr1:64744621-64744978 | Common:1; Rare:108 | ||||
chr1:64966490-64966673 | Common:1; Rare:67 | ||||
chr1:65147163-65147362 | Common:1; Rare:38 | ||||
chr1:65147804-65148345 | Common:5; Rare:114 | ||||
chr1:65148884-65149098 | Common:4; Rare:62 |