Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:231961607-231961748 | Rare:50; Clinvar:3 | ||||
chr2:232550591-232550721 | Rare:51 | ||||
chr2:232550926-232551091 | Common:1; Rare:36 | ||||
chr2:237085717-237085955 | Common:2; Rare:83 | ||||
chr2:237966728-237967083 | Common:4; Rare:110 | ||||
chr2:238060729-238061066 | Common:4; Rare:105 | ||||
chr2:239401644-239401742 | Rare:45 | ||||
chr2:240025229-240025529 | Common:3; Rare:120; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr2:240560753-240560849 | Rare:40 | ||||
chr2:240560973-240561310 | Common:4; Rare:161 | ||||
chr2:241102260-241102464 | Common:2; Rare:67 | ||||
chr2:241149422-241149646 | Common:3; Rare:74 | ||||
chr2:241239619-241240039 | Common:2; Rare:136 | ||||
chr2:241272819-241273030 | Rare:75 | ||||
chr2:241315149-241315390 | Common:4; Rare:81 |