Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:61077344-61077408 | Rare:18 | ||||
chr1:61081514-61081769 | Rare:60 | ||||
chr1:61082058-61082133 | Rare:22 | ||||
chr1:61082275-61082638 | Common:1; Rare:136 | ||||
chr1:61742369-61742521 | Rare:43 | ||||
chr1:62688266-62688510 | Common:1; Rare:99 | ||||
chr1:62784069-62784185 | Rare:48 | ||||
chr1:63367529-63367668 | Rare:41 | ||||
chr1:63523170-63523592 | Common:3; Rare:110 | ||||
chr1:63592910-63593495 | Rare:155; Clinvar (benign):1 | ||||
chr1:63593633-63593675 | Rare:20; Clinvar (pathogenic):1 | ||||
chr1:63593677-63593753 | Rare:31 | ||||
chr1:64841276-64841529 | Rare:55; Clinvar:1 | ||||
chr1:65309397-65309543 | Rare:35 | ||||
chr1:66533906-66534169 | Common:1; Rare:66 |