ID: 127886954 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:41623075-41623852 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43545707..43546484) | | |
ID: 127886953 | H3K27ac hESC enhancer GRCh37_chr17:41622297-41623074 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43544929..43545706) | | |
ID: 127886952 | H3K4me1 hESC enhancer GRCh37_chr17:41617770-41618270 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43540402..43540902) | | |
ID: 127886951 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:41605963-41606504 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43528595..43529136) | | |
ID: 127886950 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:41561036-41561878 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43483668..43484510) | | |
ID: 125177484 | Sharpr-MPRA regulatory region 5739 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43525841..43526135) | | |
ID: 124904112 | U7 small nuclear RNA [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43486398..43486458, complement) | | |
ID: 106481926 | RNA, U6 small nuclear 971, pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43473585..43473690) | | |
ID: 284064 | ribosomal protein L29 pseudogene 31 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43476154..43476765) | PERMIT, RPL29_11_1549, p17 | |
ID: 2118 | ETS variant transcription factor 4 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43527846..43546340, complement) | E1A-F, E1AF, PEA3, PEAS3 | 600711 |
ID: 1659 | DEAH-box helicase 8 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43483975..43544799) | DDX8, Dhr2, HRH1, PRP22, PRPF22 | 600396 |