Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:63367482-63367686 | Rare:64; Clinvar (benign):1 | ||||
chr1:63523170-63523592 | Common:3; Rare:110 | ||||
chr1:63593060-63593512 | Rare:136; Clinvar (benign):2 | ||||
chr1:63594204-63594250 | Common:1; Rare:7 | ||||
chr1:65147490-65147670 | Rare:56 | ||||
chr1:65148896-65149086 | Common:3; Rare:56 | ||||
chr1:65254323-65254564 | Common:2; Rare:87 | ||||
chr1:65525581-65526076 | Common:1; Rare:103 | ||||
chr1:66752322-66752535 | Rare:44 | ||||
chr1:66924808-66925041 | Rare:97 | ||||
chr1:66925188-66925503 | Common:2; Rare:99 | ||||
chr1:66958640-66958902 | Common:1; Rare:52 | ||||
chr1:67053941-67054238 | Common:2; Rare:100 | ||||
chr1:67424885-67425221 | Rare:84 | ||||
chr1:67430143-67430547 | Rare:148 |