Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:61742387-61742517 | Rare:35 | ||||
chr1:62436253-62436348 | Common:2; Rare:30 | ||||
chr1:62436789-62437103 | Common:1; Rare:82 | ||||
chr1:62688271-62688519 | Common:1; Rare:97 | ||||
chr1:62784050-62784180 | Rare:49 | ||||
chr1:63367529-63367675 | Rare:43; Clinvar (benign):1 | ||||
chr1:63523170-63523592 | Common:3; Rare:110 | ||||
chr1:63593612-63593675 | Rare:32; Clinvar (pathogenic):1 | ||||
chr1:64841310-64841529 | Rare:49; Clinvar:1 | ||||
chr1:64966385-64966651 | Common:1; Rare:92 | ||||
chr1:65148905-65149032 | Rare:37 | ||||
chr1:65254300-65254556 | Common:2; Rare:94 | ||||
chr1:65309418-65309573 | Rare:39 | ||||
chr1:66332233-66332464 | Rare:62 | ||||
chr1:66354289-66354653 | Common:1; Rare:48 |