| ID: 130063907 | ATAC-STARR-seq lymphoblastoid silent region 10320 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17079647..17079746) | | |
| ID: 130063906 | ATAC-STARR-seq lymphoblastoid silent region 10319 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17075575..17075924) | | |
| ID: 130063905 | ATAC-STARR-seq lymphoblastoid active region 14253 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17075195..17075394) | | |
| ID: 127890734 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:17192643-17193192 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17081833..17082382) | | |
| ID: 127890733 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:17190569-17191106 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17079759..17080296) | | |
| ID: 127890732 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:17137792-17138700 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17026982..17027890) | | |
| ID: 127890731 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:17072151-17072708 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (16961341..16961898) | | |
| ID: 127890730 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:17071591-17072150 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (16960781..16961340) | | |
| ID: 127890729 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:17062521-17063084 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (16951711..16952274) | | |
| ID: 125371489 | Sharpr-MPRA regulatory region 7940 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17075919..17076213) | | |
| ID: 121627860 | Sharpr-MPRA regulatory region 9643 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17049819..17050113) | | |
| ID: 109623483 | small nucleolar RNA, H/ACA box 118 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17092235..17092365) | | |
| ID: 93323 | HAUS augmin like complex subunit 8 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17049729..17075533, complement) | DGT4, HICE1, NY-SAR-48 | 613434 |
| ID: 27151 | C3 and PZP like alpha-2-macroglobulin domain containing 8 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (16892951..17026810, complement) | ASGD8, K-CAP, VIP | 608841 |
| ID: 4650 | myosin IXB [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17075777..17213286) | CELIAC4, MYR5 | 602129 |