ID: 127886928 | H3K4me1 hESC enhancer GRCh37_chr17:41142673-41143174 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (42990656..42991157) | | |
ID: 127886927 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:41124646-41125212 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (42972629..42973195) | | |
ID: 126862570 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr17:41149993-41151192 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (42997976..42999175) | | |
ID: 124904006 | uncharacterized LOC124904006 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (42992785..42999933, complement) | | |
ID: 100885850 | PTGES3L-AARSD1 readthrough [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (42950526..42980528, complement) | | |
ID: 100885848 | prostaglandin E synthase 3 like [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (42968103..42980080, complement) | | |
ID: 146923 | RUN domain containing 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (42980565..42995142) | RUND1 | 619250 |
ID: 10493 | vesicle amine transport 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43014607..43022385, complement) | VATI | 604631 |
ID: 6155 | ribosomal protein L27 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (42998273..43002959) | DBA16, L27, eL27 | 607526 |
ID: 3430 | interferon induced protein 35 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43006784..43014456) | IFP35 | 600735 |