Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:61076970-61077292 | Common:3; Rare:79 | ||||
chr1:61082409-61082816 | Common:2; Rare:135 | ||||
chr1:61403940-61404262 | Common:3; Rare:74 | ||||
chr1:61742370-61742521 | Rare:43 | ||||
chr1:62688265-62688506 | Common:1; Rare:99 | ||||
chr1:62784070-62784180 | Rare:44 | ||||
chr1:63523186-63523602 | Common:3; Rare:104 | ||||
chr1:63593624-63593692 | Rare:38; Clinvar (pathogenic):1 | ||||
chr1:64841243-64841529 | Rare:64; Clinvar:1 | ||||
chr1:65147550-65147912 | Common:1; Rare:102 | ||||
chr1:65148712-65149026 | Common:3; Rare:91 | ||||
chr1:66533492-66533643 | Common:2; Rare:23 | ||||
chr1:66534017-66534175 | Common:1; Rare:34 | ||||
chr1:66924835-66925062 | Rare:91 | ||||
chr1:66925182-66925514 | Common:2; Rare:106 |