| ID: 127891116 | H3K4me1 hESC enhancer GRCh37_chr19:30030190-30030690 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29539283..29539783) | | |
| ID: 127891115 | H3K4me1 hESC enhancer GRCh37_chr19:30025281-30025781 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29534374..29534874) | | |
| ID: 127891114 | H3K4me1 hESC enhancer GRCh37_chr19:29910274-29911005 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29419367..29420098) | | |
| ID: 127891113 | H3K4me1 hESC enhancer GRCh37_chr19:29908074-29908807 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29417167..29417900) | | |
| ID: 127891112 | H3K4me1 hESC enhancer GRCh37_chr19:29895755-29896381 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29404795..29405474) | | |
| ID: 127891111 | H3K4me1 hESC enhancer GRCh37_chr19:29863069-29863661 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29372162..29372754) | | |
| ID: 127891110 | H3K4me1 hESC enhancer GRCh37_chr19:29862474-29863068 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29371567..29372161) | | |
| ID: 127891109 | H3K4me1 hESC enhancer GRCh37_chr19:29814030-29814530 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29323123..29323623) | | |
| ID: 127891108 | H3K4me1 hESC enhancer GRCh37_chr19:29802585-29803084 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29311678..29312177) | | |
| ID: 127891107 | H3K4me1 hESC enhancer GRCh37_chr19:29802083-29802584 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29311176..29311677) | | |
| ID: 127891106 | H3K4me1 hESC enhancer GRCh37_chr19:29799690-29800520 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29308783..29309613) | | |
| ID: 124904683 | uncharacterized LOC124904683 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29488179..29529280, complement) | | |
| ID: 113939969 | Sharpr-MPRA regulatory region 9443 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29415562..29415856) | | |
| ID: 106481016 | RNA, 7SL, cytoplasmic 340, pseudogene [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29233090..29233385, complement) | | |
| ID: 105372352 | UQCRFS1 divergent transcript [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29213253..29215815) | CTB-32O4.2, CTB-32O4.3, CTB-32O4.4 | |
| ID: 342865 | V-set and transmembrane domain containing 2B [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29525418..29564551) | | |
| ID: 284395 | VSTM2B divergent transcript [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29287009..29525750, complement) | | |