| ID: 130064167 | ATAC-STARR-seq lymphoblastoid active region 14436 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32972366..32972415) | | |
| ID: 130064166 | ATAC-STARR-seq lymphoblastoid silent region 10487 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32972096..32972225) | | |
| ID: 130064165 | ATAC-STARR-seq lymphoblastoid active region 14435 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32971766..32971985) | | |
| ID: 127891192 | H3K27ac hESC enhancer GRCh37_chr19:33539186-33539904 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (33048280..33048998) | | |
| ID: 127891191 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:33534226-33534776 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (33043320..33043870) | | |
| ID: 127891190 | H3K4me1 hESC enhancer GRCh37_chr19:33532539-33533040 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (33041633..33042134) | | |
| ID: 127891189 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:33522974-33523845 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (33032068..33032939) | | |
| ID: 127891188 | H3K4me1 hESC enhancer GRCh37_chr19:33427027-33427526 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32936121..32936620) | | |
| ID: 127891187 | H3K4me1 hESC enhancer GRCh37_chr19:33426525-33427026 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32935619..32936120) | | |
| ID: 127891186 | H3K4me1 hESC enhancer GRCh37_chr19:33366062-33366947 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32875156..32876041) | | |
| ID: 127891185 | H3K4me1 hESC enhancer GRCh37_chr19:33361501-33362023 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32870595..32871117) | | |
| ID: 127891184 | H3K4me1 hESC enhancer GRCh37_chr19:33360978-33361500 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32870072..32870594) | | |
| ID: 127891183 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:33358961-33359536 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32868055..32868630) | | |
| ID: 127891182 | H3K4me1 hESC enhancer GRCh37_chr19:33319941-33320462 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32829035..32829556) | | |
| ID: 124904805 | uncharacterized LOC124904805 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (33051403..33051504) | | |
| ID: 111413028 | HNF1 motif-containing MPRA enhancer 165 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (33041357..33041501) | | |
| ID: 106481805 | RN7SK pseudogene 22 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32862800..32863092, complement) | | |
| ID: 100421414 | GCM1 pseudogene 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32823436..32824505, complement) | | |
| ID: 100271486 | ribosomal protein L31 pseudogene 60 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32963508..32963865) | RPL31_33_1645 | |
| ID: 91646 | tudor domain containing 12 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32719767..32829580) | ECAT8 | |