Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:232550514-232550721 | Rare:85 | ||||
chr2:232550956-232551110 | Common:1; Rare:28 | ||||
chr2:237085819-237085976 | Common:1; Rare:66 | ||||
chr2:237413954-237414328 | Common:2; Rare:74; Clinvar (benign):3 | ||||
chr2:237487167-237487287 | Common:2; Rare:35 | ||||
chr2:238060748-238061121 | Common:6; Rare:120 | ||||
chr2:238426880-238427021 | Common:1; Rare:48 | ||||
chr2:240560760-240560845 | Rare:36 | ||||
chr2:240561015-240561294 | Common:4; Rare:130 | ||||
chr2:241149431-241149686 | Common:4; Rare:87 | ||||
chr2:241246802-241247126 | Common:1; Rare:82 | ||||
chr2:241315171-241315459 | Common:5; Rare:95 | ||||
chr2:241315646-241315985 | Common:5; Rare:133 | ||||
chr2:241508273-241508482 | Common:1; Rare:50 | ||||
chr2:241636982-241637223 | Common:1; Rare:86 |