| ID: 127892137 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:53201006-53201816 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (52697753..52698563) | | |
| ID: 127892136 | H3K27ac hESC enhancer GRCh37_chr19:53199383-53200194 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (52696130..52696941) | | |
| ID: 127892135 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:53196613-53197148 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (52693360..52693895) | | |
| ID: 127892134 | H3K27ac hESC enhancer GRCh37_chr19:53192883-53193418 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (52689630..52690165) | | |
| ID: 127892133 | NANOG-H3K27ac hESC enhancer GRCh37_chr19:53179901-53180465 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (52676648..52677212) | | |
| ID: 127892132 | H3K27ac hESC enhancer GRCh37_chr19:53179336-53179900 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (52676083..52676647) | | |
| ID: 127892131 | H3K4me1 hESC enhancer GRCh37_chr19:53177263-53177762 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (52674010..52674509) | | |
| ID: 127892130 | H3K27ac hESC enhancer GRCh37_chr19:53171845-53172346 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (52668592..52669093) | | |
| ID: 127892129 | H3K4me1 hESC enhancer GRCh37_chr19:53167404-53167904 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (52664151..52664651) | | |
| ID: 127892128 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:53141055-53141572 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (52637802..52638319) | | |
| ID: 127892127 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:53140536-53141054 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (52637283..52637801) | | |
| ID: 127892126 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:53104606-53105112 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (52601341..52601859) | | |
| ID: 126862927 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr19:53172853-53174052 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (52669600..52670799) | | |
| ID: 125384532 | Sharpr-MPRA regulatory region 1800 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (52648576..52648870) | | |
| ID: 124908087 | uncharacterized LOC124908087 [Homo sapiens (human)] | | | |
| ID: 124904757 | zinc finger protein 677-like [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (52618375..52638355, complement) | | |
| ID: 122539214 | Zinc finger protein LOC122539214 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (52650447..52690496, complement) | | |
| ID: 55769 | zinc finger protein 83 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (52612377..52690496, complement) | HPF1, ZNF816B | 194558 |
| ID: 55762 | zinc finger protein 701 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (52570287..52600149) | | |
| ID: 7696 | zinc finger protein 137, pseudogene [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (52596684..52600152) | ZNF137, pHZ-30 | 604079 |