Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161045834-161046096 | Common:1; Rare:72 | ||||
chr1:161098264-161098405 | Common:1; Rare:23 | ||||
chr1:161117397-161117797 | Common:1; Rare:130 | ||||
chr1:161117997-161118196 | Rare:105 | ||||
chr1:161132426-161132607 | Rare:63 | ||||
chr1:161132734-161133102 | Common:2; Rare:82 | ||||
chr1:161133120-161133510 | Common:2; Rare:61 | ||||
chr1:161153898-161154260 | Rare:123; Clinvar (pathogenic):1 | ||||
chr1:161159356-161159572 | Common:2; Rare:67 | ||||
chr1:161159760-161159969 | Common:2; Rare:50 | ||||
chr1:161166228-161166512 | Common:2; Rare:77; Clinvar:3; Clinvar (benign):1 | ||||
chr1:161177457-161177585 | Rare:52 | ||||
chr1:161202183-161202466 | Common:2; Rare:96; Clinvar:3; Clinvar (benign):7 | ||||
chr1:161202481-161202881 | Common:4; Rare:116; Clinvar:1; Clinvar (benign):2 | ||||
chr1:161225714-161226067 | Common:10; Rare:53 |