Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:86105831-86106183 | Common:2; Rare:89 | ||||
chr2:86195387-86195547 | Common:5; Rare:57 | ||||
chr2:86199403-86199497 | Common:1; Rare:35 | ||||
chr2:86441069-86441396 | Common:1; Rare:109 | ||||
chr2:88055736-88055923 | Rare:69 | ||||
chr2:88691450-88691885 | Common:2; Rare:164; Clinvar:1 | ||||
chr2:95121778-95122084 | Rare:94 | ||||
chr2:95165651-95165828 | Rare:54 | ||||
chr2:95207447-95207538 | Rare:34 | ||||
chr2:95402583-95402754 | Rare:56 | ||||
chr2:96208274-96208418 | Rare:71 | ||||
chr2:96208805-96208942 | Common:3; Rare:50 | ||||
chr2:96265968-96266296 | Common:2; Rare:96; Clinvar:1 | ||||
chr2:96305475-96305609 | Common:1; Rare:45; Clinvar:2; Clinvar (benign):2 | ||||
chr2:96325238-96325343 | Rare:26 |