Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:218275453-218275774 | Common:3; Rare:100 | ||||
chr2:218277037-218277358 | Common:2; Rare:80 | ||||
chr2:218277364-218277729 | Rare:102 | ||||
chr2:218370618-218370871 | Rare:45 | ||||
chr2:218402634-218402714 | Rare:25 | ||||
chr2:221573081-221573236 | Common:1; Rare:34 | ||||
chr2:226172394-226172566 | Rare:33 | ||||
chr2:226795965-226796270 | Common:2; Rare:102 | ||||
chr2:226796768-226797001 | Rare:68; Clinvar (pathogenic):1 | ||||
chr2:226797351-226797648 | Common:1; Rare:99 | ||||
chr2:226798429-226798634 | Common:1; Rare:67 | ||||
chr2:231393712-231393789 | Rare:13 | ||||
chr2:231514320-231514583 | Common:5; Rare:105 | ||||
chr2:231604633-231604931 | Common:21; Rare:109 | ||||
chr2:232584370-232584512 | Common:1; Rare:27 |