Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:54199999-54200214 | Rare:50 | ||||
chr1:55215357-55215414 | Rare:29 | ||||
chr1:56645245-56645394 | Common:1; Rare:56 | ||||
chr1:58783991-58784175 | Rare:39 | ||||
chr1:59296520-59296831 | Common:12; Rare:80 | ||||
chr1:62688254-62688482 | Common:1; Rare:95; Clinvar:1 | ||||
chr1:62784068-62784172 | Rare:42 | ||||
chr1:63523152-63523581 | Common:3; Rare:119 | ||||
chr1:65420582-65420734 | Common:3; Rare:53; Clinvar:2; Clinvar (benign):1 | ||||
chr1:66533559-66534190 | Common:2; Rare:146 | ||||
chr1:66924808-66925036 | Rare:96 | ||||
chr1:66925204-66925333 | Common:2; Rare:39 | ||||
chr1:70205542-70205764 | Rare:72 | ||||
chr1:70354684-70354854 | Rare:62 | ||||
chr1:71066700-71066875 | Rare:62 |