ID: 127883634 | H3K4me1 hESC enhancer GRCh37_chr16:30064875-30065853 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (30053554..30054532) | | |
ID: 127883633 | H3K4me1 hESC enhancer GRCh37_chr16:30039801-30040645 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (30028480..30029324) | | |
ID: 127883632 | H3K4me1 hESC enhancer GRCh37_chr16:30015046-30015830 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (30003725..30004509) | | |
ID: 127883631 | H3K4me1 hESC enhancer GRCh37_chr16:30004929-30005429 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29993608..29994108) | | |
ID: 112694756 | uncharaterized LOC112694756 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (30053151..30070414) | ALDA, ALDOA | |
ID: 283899 | INO80 complex subunit E [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29996241..30005791) | CCDC95 | |
ID: 146378 | chromosome 16 open reading frame 92 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (30023198..30027736) | FIMP | 618911 |
ID: 83723 | TLC domain containing 3B [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (30024427..30053040, complement) | CORD22, FAM57B, FP1188 | 615175 |
ID: 8479 | HIRA interacting protein 3 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29992321..29996096, complement) | | 603365 |
ID: 8448 | double C2 domain alpha [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (30005514..30023228, complement) | Doc2 | 604567 |