Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:63593705-63593833 | Common:2; Rare:56 | ||||
chr1:66332137-66332464 | Rare:79 | ||||
chr1:66533877-66534161 | Common:2; Rare:70 | ||||
chr1:66924774-66925041 | Common:2; Rare:117 | ||||
chr1:66925149-66925349 | Common:2; Rare:63 | ||||
chr1:66930019-66930397 | Rare:126 | ||||
chr1:67053941-67053992 | Rare:22 | ||||
chr1:67054078-67054332 | Common:2; Rare:48 | ||||
chr1:70205533-70205763 | Rare:77 | ||||
chr1:70221278-70221670 | Rare:152 | ||||
chr1:70354648-70354856 | Rare:70 | ||||
chr1:70411069-70411303 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080997-71081373 | Rare:96 | ||||
chr1:74198148-74198270 | Common:1; Rare:63 | ||||
chr1:76867367-76867501 | Rare:35 |