Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:189783965-189784085 | Common:3; Rare:42; Clinvar (benign):1 | ||||
chr2:189784275-189784560 | Common:4; Rare:100; Clinvar:8; Clinvar (benign):2 | ||||
chr2:190343952-190344043 | Rare:19 | ||||
chr2:190534687-190534870 | Common:1; Rare:60 | ||||
chr2:191014115-191014368 | Common:2; Rare:93; Clinvar:2; Clinvar (benign):2 | ||||
chr2:191677848-191678201 | Common:4; Rare:99 | ||||
chr2:196799613-196799823 | Common:2; Rare:66 | ||||
chr2:197434980-197435176 | Rare:66 | ||||
chr2:197453247-197453557 | Rare:104 | ||||
chr2:197499794-197500461 | Common:1; Rare:255; Clinvar:1; Clinvar (benign):1 | ||||
chr2:197515780-197516107 | Common:2; Rare:113 | ||||
chr2:200509901-200510210 | Common:1; Rare:110 | ||||
chr2:200585867-200586103 | Rare:61 | ||||
chr2:200811377-200811589 | Common:1; Rare:72 | ||||
chr2:200811818-200811972 | Rare:68 |