Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:71130220-71130666 | Common:6; Rare:125; Clinvar:1; Clinvar (benign):2 | ||||
chr2:71276450-71276602 | Rare:47 | ||||
chr2:73071694-73071841 | Common:2; Rare:58 | ||||
chr2:73284445-73284524 | Rare:16 | ||||
chr2:73828801-73829028 | Common:1; Rare:52 | ||||
chr2:74147821-74148149 | Common:2; Rare:87; Clinvar:2; Clinvar (benign):2 | ||||
chr2:74198490-74198617 | Rare:51 | ||||
chr2:74421571-74421772 | Rare:68 | ||||
chr2:74454865-74455139 | Rare:76 | ||||
chr2:74458085-74458519 | Common:1; Rare:133 | ||||
chr2:74465329-74465470 | Common:1; Rare:38; Clinvar:1 | ||||
chr2:74529659-74530036 | Rare:113; Clinvar:3; Clinvar (benign):1 | ||||
chr2:74554411-74554766 | Common:2; Rare:108 | ||||
chr2:74833805-74834139 | Common:1; Rare:100 | ||||
chr2:74835141-74835324 | Rare:49 |