| ID: 130064193 | ATAC-STARR-seq lymphoblastoid silent region 10505 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34501810..34501869) | | |
| ID: 130064192 | ATAC-STARR-seq lymphoblastoid silent region 10504 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34428719..34428878) | | |
| ID: 130064191 | ATAC-STARR-seq lymphoblastoid silent region 10503 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34428539..34428648) | | |
| ID: 130064190 | ATAC-STARR-seq lymphoblastoid silent region 10502 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34428269..34428508) | | |
| ID: 129664425 | ReSE screen-validated silencer GRCh37_chr19:34928566-34928723 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34437661..34437818) | | |
| ID: 129391094 | MPRA-validated peak3443 silencer [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34452991..34453191) | | |
| ID: 127891259 | H3K4me1 hESC enhancer GRCh37_chr19:34996657-34997157 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34505752..34506252) | | |
| ID: 127891258 | H3K4me1 hESC enhancer GRCh37_chr19:34996156-34996656 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34505251..34505751) | | |
| ID: 127891257 | H3K4me1 hESC enhancer GRCh37_chr19:34994324-34995145 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34503419..34504240) | | |
| ID: 127891256 | H3K4me1 hESC enhancer GRCh37_chr19:34989177-34990063 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34498272..34499158) | | |
| ID: 127891255 | H3K4me1 hESC enhancer GRCh37_chr19:34988289-34989176 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34497384..34498271) | | |
| ID: 127891254 | H3K27ac hESC enhancer GRCh37_chr19:34973047-34973701 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34482142..34482796) | | |
| ID: 127891253 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:34972391-34973046 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34481486..34482141) | | |
| ID: 127891252 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:34971736-34972390 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34480831..34481485) | | |
| ID: 124904695 | uncharacterized LOC124904695 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34426106..34428364, complement) | | |
| ID: 106479277 | RNA, 7SL, cytoplasmic 154, pseudogene [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34421988..34422311, complement) | | |
| ID: 105372374 | uncharacterized LOC105372374 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34555494..34558984) | | |
| ID: 100129800 | zinc finger protein 807, pseudogene [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34541692..34677159, complement) | ZNF181P1, ZNF807 | |
| ID: 100129650 | ribosomal protein S26 pseudogene 55 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34533358..34534113, complement) | RPS26_30_1651 | |
| ID: 126374 | WT1 interacting protein [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34481758..34512304) | | 614790 |