Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:24049592-24049743 | Rare:41 | ||||
chr2:24076238-24076500 | Rare:78 | ||||
chr2:24084374-24084696 | Common:5; Rare:77 | ||||
chr2:24123252-24123504 | Common:1; Rare:67 | ||||
chr2:25878457-25878654 | Common:1; Rare:61 | ||||
chr2:26033774-26034159 | Common:4; Rare:140 | ||||
chr2:26244581-26244963 | Common:2; Rare:140; Clinvar:5; Clinvar (benign):9 | ||||
chr2:26345841-26346165 | Common:1; Rare:96 | ||||
chr2:26764188-26764325 | Common:1; Rare:53 | ||||
chr2:27032867-27033004 | Rare:51 | ||||
chr2:27211935-27212103 | Common:3; Rare:62 | ||||
chr2:27212271-27212367 | Common:1; Rare:48 | ||||
chr2:27323047-27323136 | Rare:21; Clinvar (benign):1 | ||||
chr2:27356750-27357034 | Rare:75 | ||||
chr2:27370282-27370641 | Common:1; Rare:149 |