Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:6918646-6918830 | Common:4; Rare:39 | ||||
chr2:8583792-8584044 | Common:3; Rare:76 | ||||
chr2:15941673-15941830 | Common:1; Rare:44 | ||||
chr2:20448385-20448600 | Common:1; Rare:60 | ||||
chr2:25822104-25822349 | Common:6; Rare:55 | ||||
chr2:34677825-34677898 | Common:3; Rare:21 | ||||
chr2:36544073-36544495 | Common:4; Rare:115 | ||||
chr2:37216159-37216244 | Rare:27 | ||||
chr2:37992778-37992885 | Rare:26 | ||||
chr2:38071309-38071568 | Common:1; Rare:49 | ||||
chr2:40209072-40209335 | Common:2; Rare:68 | ||||
chr2:42295232-42295472 | Rare:66 | ||||
chr2:47335308-47335323 | Rare:6 | ||||
chr2:47803166-47803446 | Common:1; Rare:95; Clinvar:6; Clinvar (benign):12 | ||||
chr2:47906476-47906818 | Common:2; Rare:123 |