Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:186485987-186486344 | Common:3; Rare:99 | ||||
chr2:188974185-188974568 | Rare:93; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr2:189007862-189008140 | Rare:88; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):16 | ||||
chr2:189441133-189441501 | Common:2; Rare:107 | ||||
chr2:189783957-189784098 | Common:3; Rare:48; Clinvar (benign):1 | ||||
chr2:189784275-189784547 | Common:4; Rare:99; Clinvar:8; Clinvar (benign):2 | ||||
chr2:191246159-191246305 | Common:1; Rare:42 | ||||
chr2:191677828-191678161 | Common:4; Rare:95 | ||||
chr2:192194905-192195178 | Common:1; Rare:67 | ||||
chr2:197434986-197435198 | Rare:70 | ||||
chr2:197453244-197453549 | Rare:101 | ||||
chr2:197499811-197500430 | Common:1; Rare:238; Clinvar:1; Clinvar (benign):1 | ||||
chr2:200306364-200306562 | Common:3; Rare:45 | ||||
chr2:200510040-200510141 | Rare:32 | ||||
chr2:200864617-200864784 | Rare:63 |