| ID: 130063624 | ATAC-STARR-seq lymphoblastoid silent region 10143 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12092483..12092712) | | |
| ID: 130063623 | ATAC-STARR-seq lymphoblastoid silent region 10142 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12092113..12092172) | | |
| ID: 130063622 | ATAC-STARR-seq lymphoblastoid silent region 10141 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12064996..12065175) | | |
| ID: 130063621 | ATAC-STARR-seq lymphoblastoid active region 14043 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12064816..12064905) | | |
| ID: 130063620 | ATAC-STARR-seq lymphoblastoid silent region 10140 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12052557..12052606) | | |
| ID: 130063619 | ATAC-STARR-seq lymphoblastoid silent region 10139 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12035634..12035793) | | |
| ID: 130063618 | ATAC-STARR-seq lymphoblastoid silent region 10138 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12035344..12035393) | | |
| ID: 130063617 | ATAC-STARR-seq lymphoblastoid silent region 10137 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12035214..12035333) | | |
| ID: 130063616 | ATAC-STARR-seq lymphoblastoid active region 14042 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12000694..12000743) | | |
| ID: 130063615 | ATAC-STARR-seq lymphoblastoid silent region 10136 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (11965260..11965459) | | |
| ID: 127890509 | H3K27ac hESC enhancer GRCh37_chr19:12163610-12164115 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12052795..12053300) | | |
| ID: 127890508 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:12099227-12100168 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (11988412..11989353) | | |
| ID: 127890507 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:12098284-12099226 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (11987469..11988411) | | |
| ID: 112543445 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:12074983-12075936 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (11964168..11965121) | | |
| ID: 101928464 | ZNF433 and ZNF878 antisense RNA 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (11987617..12046275) | | |
| ID: 100873710 | RNA, 5S ribosomal pseudogene 466 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12070164..12070271) | RN5S466 | |
| ID: 100873709 | RNA, 5S ribosomal pseudogene 465 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12027913..12028021, complement) | RN5S465 | |
| ID: 100873708 | RNA, 5S ribosomal pseudogene 464 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (11996809..11996916) | RN5S464 | |
| ID: 100462809 | ribosomal L24 domain containing 1 pseudogene 8 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12096380..12097109) | | |
| ID: 100127050 | vomeronasal 2 receptor 21 pseudogene [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (11953189..11953474, complement) | | |