| ID: 130064943 | ATAC-STARR-seq lymphoblastoid active region 14958 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49817848..49818207) | | |
| ID: 130064942 | ATAC-STARR-seq lymphoblastoid silent region 10936 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49809327..49809496) | | |
| ID: 130064941 | ATAC-STARR-seq lymphoblastoid active region 14955 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49809047..49809146) | | |
| ID: 129664506 | ReSE screen-validated silencer GRCh37_chr19:50321502-50321668 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49818245..49818497) | | |
| ID: 129664505 | ReSE screen-validated silencer GRCh37_chr19:50263738-50263955 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49760481..49760698) | | |
| ID: 127892024 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:50316420-50317226 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49813163..49813969) | | |
| ID: 127892023 | H3K4me1 hESC enhancer GRCh37_chr19:50306331-50306844 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49803074..49803587) | | |
| ID: 127892022 | H3K4me1 hESC enhancer GRCh37_chr19:50305815-50306330 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49802558..49803073) | | |
| ID: 127892021 | H3K4me1 hESC enhancer GRCh37_chr19:50303481-50303981 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49800224..49800724) | | |
| ID: 127892020 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:50274662-50275586 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49771405..49772329) | | |
| ID: 127892018 | hESC enhancers GRCh37_chr19:50268923-50269900 and GRCh37_chr19:50269954-50270722 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49765666..49767465) | | |
| ID: 127892017 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:50264724-50265316 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49761467..49762059) | | |
| ID: 124904742 | uncharacterized LOC124904742 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49797346..49800150, complement) | | |
| ID: 106480699 | RNA, U6 small nuclear 841, pseudogene [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49764525..49764630, complement) | | |
| ID: 105372435 | uncharacterized LOC105372435 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49808920..49809826) | | |
| ID: 105372434 | uncharacterized LOC105372434 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49748142..49757879) | | |
| ID: 102465480 | microRNA 6800 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49832018..49832099) | hsa-mir-6800 | |
| ID: 102465479 | microRNA 6799 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49791866..49791934) | hsa-mir-6799 | |
| ID: 81857 | mediator complex subunit 25 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49818289..49840384) | ACID1, ARC92, BVSYS, CMT2B2, P78, PTOV2, TCBAP0758 | 610197 |
| ID: 80199 | fuzzy planar cell polarity protein [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49806866..49813553, complement) | CPLANE3, FY, NTD | 610622 |