ID: 127882972 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:4441217-4441770 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (4391216..4391769) | | |
ID: 127882971 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:4440665-4441216 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (4390664..4391215) | | |
ID: 127882970 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:4433428-4434269 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (4383427..4384268) | | |
ID: 127882969 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:4428659-4429440 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (4378658..4379439) | | |
ID: 127882968 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:4426319-4427098 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (4376318..4377097) | | |
ID: 127882967 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:4425537-4426318 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (4375536..4376317) | | |
ID: 127882966 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:4424664-4425443 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (4374663..4375442) | | |
ID: 127882965 | H3K4me1 hESC enhancer GRCh37_chr16:4421231-4422056 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (4371230..4372055) | | |
ID: 127882964 | H3K4me1 hESC enhancer GRCh37_chr16:4419155-4419654 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (4369154..4369653) | | |
ID: 127882963 | H3K4me1 hESC enhancer GRCh37_chr16:4415328-4415828 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (4365327..4365827) | | |
ID: 127882962 | H3K4me1 hESC enhancer GRCh37_chr16:4397350-4397850 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (4347349..4347849) | | |
ID: 100529144 | CORO7-PAM16 readthrough [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (4340251..4416596, complement) | CORO7, Coronin-7, Crn7 | |
ID: 114990 | vasorin [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (4371848..4383538) | SLITL2 | 608843 |
ID: 79585 | coronin 7 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (4354542..4416596, complement) | 0610011B16Rik, CRN7, POD1 | 611668 |
ID: 51025 | presequence translocase associated motor 16 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (4340251..4351321, complement) | CGI-136, MAGMAS, SMDMDM, TIM16, TIMM16 | 614336 |