| ID: 130064904 | ATAC-STARR-seq lymphoblastoid active region 14927 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49149523..49149742) | | |
| ID: 130064903 | ATAC-STARR-seq lymphoblastoid silent region 10914 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49127873..49128272) | | |
| ID: 130064902 | ATAC-STARR-seq lymphoblastoid silent region 10913 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49119155..49119374) | | |
| ID: 130064901 | ATAC-STARR-seq lymphoblastoid silent region 10912 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49114190..49114769) | | |
| ID: 130064900 | ATAC-STARR-seq lymphoblastoid active region 14926 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49085547..49085636) | | |
| ID: 130064899 | ATAC-STARR-seq lymphoblastoid active region 14925 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49085127..49085196) | | |
| ID: 129664496 | ReSE screen-validated silencer GRCh37_chr19:49577315-49577474 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49074058..49074217) | | |
| ID: 127891972 | H3K4me1 hESC enhancer GRCh37_chr19:49644909-49645502 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49141652..49142245) | | |
| ID: 127891971 | H3K4me1 hESC enhancer GRCh37_chr19:49640079-49640585 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49136822..49137328) | | |
| ID: 127891970 | H3K4me1 hESC enhancer GRCh37_chr19:49635887-49636531 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49132630..49133274) | | |
| ID: 127891969 | H3K4me1 hESC enhancer GRCh37_chr19:49623585-49624085 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49120328..49120828) | | |
| ID: 127891968 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:49621711-49622222 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49118454..49118965) | | |
| ID: 127891967 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:49610053-49610894 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49106796..49107637) | | |
| ID: 127891966 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:49604029-49604882 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49100772..49101625) | | |
| ID: 127891965 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:49603173-49604028 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49099916..49100771) | | |
| ID: 127891964 | H3K4me1 hESC enhancer GRCh37_chr19:49575349-49575848 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49072092..49072591) | | |
| ID: 127891963 | H3K4me1 hESC enhancer GRCh37_chr19:49574847-49575348 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49071590..49072091) | | |
| ID: 106479481 | RNA, 7SL, cytoplasmic 708, pseudogene [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49081332..49081630) | | |
| ID: 64130 | lin-7 homolog B, crumbs cell polarity complex component [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49114370..49118460) | LIN-7B, MALS-2, MALS2, VELI2 | 612331 |
| ID: 55150 | chromosome 19 open reading frame 73 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49118402..49119143, complement) | | |