Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:53838247-53838324 | Rare:35 | ||||
chr1:53889749-53889977 | Common:2; Rare:75 | ||||
chr1:53946260-53946494 | Common:1; Rare:85 | ||||
chr1:54053389-54053672 | Common:5; Rare:93 | ||||
chr1:54199988-54200215 | Rare:54 | ||||
chr1:54764500-54764821 | Common:7; Rare:88 | ||||
chr1:56516996-56517126 | Common:1; Rare:19 | ||||
chr1:59296531-59296833 | Common:12; Rare:77 | ||||
chr1:61081870-61082010 | Rare:40 | ||||
chr1:61725105-61725180 | Rare:40 | ||||
chr1:62784069-62784180 | Rare:44 | ||||
chr1:63367461-63367675 | Rare:67; Clinvar (benign):1 | ||||
chr1:63523161-63523589 | Common:3; Rare:117 | ||||
chr1:63593232-63593467 | Rare:86; Clinvar (benign):1 | ||||
chr1:66924845-66925024 | Rare:77 |