ID: 129993375 | ATAC-STARR-seq lymphoblastoid active region 22146 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (170027481..170027620) | | |
ID: 129993374 | ATAC-STARR-seq lymphoblastoid silent region 15797 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (170026373..170026772) | | |
ID: 129993373 | ATAC-STARR-seq lymphoblastoid silent region 15796 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (170026203..170026292) | | |
ID: 127401912 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:170966616-170967155 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (170045465..170046004) | | |
ID: 127401911 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:170947923-170948642 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (170026772..170027491) | | |
ID: 127401910 | H3K4me1 hESC enhancer GRCh37_chr4:170897057-170897800 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (169975906..169976649) | | |
ID: 127401909 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:170845115-170845639 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (169923964..169924488) | | |
ID: 127401908 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr4:170840735-170841282 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (169919584..169920131) | | |
ID: 127401907 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr4:170840189-170840734 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (169919038..169919583) | | |
ID: 124900810 | uncharacterized LOC124900810 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (169849051..169867335, complement) | | |
ID: 107986326 | uncharacterized LOC107986326 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (170062730..170066706) | | |
ID: 105377530 | uncharacterized LOC105377530 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (169912718..169941684) | | |
ID: 101928198 | uncharacterized LOC101928198 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (170031774..170033003, complement) | | |
ID: 100506085 | long intergenic non-protein coding RNA 2275 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (169917761..169975902, complement) | | |
ID: 402192 | chloride nucleotide-sensitive channel 1A pseudogene [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (169832564..169833386) | | |
ID: 51166 | aminoadipate aminotransferase [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (170060222..170094292, complement) | KAT2, KATII, KYAT2 | 611754 |
ID: 9848 | microfibril associated protein 3 like [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (169986602..170027277, complement) | NYD-sp9 | 616523 |