Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:61952261-61952364 | Common:3; Rare:32 | ||||
chr1:62436256-62436364 | Common:2; Rare:36 | ||||
chr1:62688271-62688544 | Common:1; Rare:103 | ||||
chr1:62784041-62784187 | Rare:61 | ||||
chr1:63367522-63367675 | Rare:45; Clinvar (benign):1 | ||||
chr1:63523158-63523597 | Common:3; Rare:120 | ||||
chr1:63593266-63593506 | Rare:93; Clinvar (benign):1 | ||||
chr1:63593640-63593692 | Rare:29; Clinvar (pathogenic):1 | ||||
chr1:63773836-63774104 | Rare:59 | ||||
chr1:64966372-64966670 | Common:2; Rare:104 | ||||
chr1:65148020-65148204 | Common:4; Rare:42 | ||||
chr1:65309186-65309582 | Common:1; Rare:97 | ||||
chr1:65420497-65420739 | Common:4; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
chr1:66354289-66354659 | Common:1; Rare:49 | ||||
chr1:66533358-66533624 | Common:2; Rare:35 |