Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:226939985-226940357 | Rare:131; Clinvar:3 | ||||
chr1:227735231-227735488 | Common:3; Rare:150 | ||||
chr1:228082498-228082765 | Common:3; Rare:110 | ||||
chr1:228103282-228103483 | Common:1; Rare:70 | ||||
chr1:228109235-228109468 | Rare:80 | ||||
chr1:228139876-228140087 | Common:1; Rare:50 | ||||
chr1:228457854-228458113 | Common:1; Rare:85 | ||||
chr1:229271027-229271315 | Rare:95 | ||||
chr1:229508199-229508462 | Common:1; Rare:101 | ||||
chr1:229625635-229625858 | Rare:48 | ||||
chr1:229625902-229626261 | Rare:115 | ||||
chr1:230978753-230979115 | Common:2; Rare:139 | ||||
chr1:231241101-231241452 | Common:3; Rare:163; Clinvar:6; Clinvar (benign):3 | ||||
chr1:231337823-231338056 | Common:2; Rare:84 | ||||
chr1:231528515-231528738 | Common:2; Rare:79 |