Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:189783965-189784085 | Common:3; Rare:42; Clinvar (benign):1 | ||||
chr2:189784271-189784512 | Common:3; Rare:81; Clinvar:7; Clinvar (benign):1 | ||||
chr2:190534696-190534876 | Common:1; Rare:59 | ||||
chr2:191014123-191014415 | Common:3; Rare:106; Clinvar:2; Clinvar (benign):2 | ||||
chr2:191677856-191678155 | Common:4; Rare:86 | ||||
chr2:197434975-197435205 | Rare:77 | ||||
chr2:197453214-197453571 | Rare:123 | ||||
chr2:197499807-197500427 | Common:1; Rare:238; Clinvar:1; Clinvar (benign):1 | ||||
chr2:197515782-197516118 | Common:2; Rare:117 | ||||
chr2:199911104-199911451 | Rare:122 | ||||
chr2:200510040-200510249 | Common:1; Rare:64 | ||||
chr2:200526011-200526225 | Common:2; Rare:66 | ||||
chr2:200609105-200609246 | Rare:35 | ||||
chr2:200811366-200811589 | Common:1; Rare:74 | ||||
chr2:200888994-200889455 | Common:3; Rare:146 |