| ID: 127891721 | H3K4me1 hESC enhancer GRCh37_chr19:45658871-45659588 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (45155613..45156330) | | |
| ID: 127891720 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:45656063-45656688 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (45152805..45153430) | | |
| ID: 127891719 | H3K4me1 hESC enhancer GRCh37_chr19:45641146-45641718 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (45137888..45138460) | | |
| ID: 127891718 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:45638457-45639261 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (45135199..45136003) | | |
| ID: 127891717 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:45632987-45633488 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (45129729..45130230) | | |
| ID: 127891716 | H3K4me1 hESC enhancer GRCh37_chr19:45619689-45620344 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (45116431..45117086) | | |
| ID: 127891715 | H3K4me1 hESC enhancer GRCh37_chr19:45608463-45609052 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (45105205..45105794) | | |
| ID: 127891714 | H3K4me1 hESC enhancer GRCh37_chr19:45603163-45603750 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (45099905..45100492) | | |
| ID: 127891713 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:45601395-45601984 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (45098137..45098726) | | |
| ID: 127891712 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:45600806-45601394 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (45097548..45098136) | | |
| ID: 127891711 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:45594045-45595039 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (45090787..45091781) | | |
| ID: 127891710 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:45593049-45594044 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (45089676..45090786) | | |
| ID: 125371527 | Sharpr-MPRA regulatory region 10789 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (45130251..45130545) | | |
| ID: 105372420 | uncharacterized LOC105372420 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (45153579..45157364) | | |
| ID: 105372419 | GEMIN7 antisense RNA 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (45085329..45090391, complement) | | |
| ID: 284353 | NTPase KAP family P-loop domain containing 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (45149744..45162841, complement) | | |
| ID: 284352 | protein phosphatase 1 regulatory subunit 37 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (45093179..45147285) | LRRC68 | |
| ID: 79760 | gem nuclear organelle associated protein 7 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (45075627..45091518) | SIP3 | 607419 |
| ID: 1987 | eukaryotic translation initiation factor 5A pseudogene 3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (45128458..45129281) | | |