Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:189441094-189441504 | Common:2; Rare:120 | ||||
chr2:189580736-189580925 | Common:1; Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
chr2:189783955-189784111 | Common:3; Rare:54; Clinvar (benign):1 | ||||
chr2:189784260-189784557 | Common:4; Rare:104; Clinvar:8; Clinvar (benign):3 | ||||
chr2:190180713-190180881 | Rare:52 | ||||
chr2:190343650-190343935 | Rare:75 | ||||
chr2:190343961-190344031 | Rare:14 | ||||
chr2:190880674-190880834 | Common:2; Rare:56 | ||||
chr2:191014116-191014350 | Common:2; Rare:80; Clinvar:2; Clinvar (benign):2 | ||||
chr2:191245219-191245555 | Common:3; Rare:111 | ||||
chr2:191263191-191263369 | Rare:31 | ||||
chr2:191677831-191678173 | Common:4; Rare:99 | ||||
chr2:191847072-191847381 | Rare:51 | ||||
chr2:196926695-196926799 | Common:2; Rare:37 | ||||
chr2:197434963-197435198 | Rare:78 |