| ID: 130062249 | ATAC-STARR-seq lymphoblastoid active region 13136 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (21612373..21612462) | | |
| ID: 130062248 | ATAC-STARR-seq lymphoblastoid silent region 9341 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (21612063..21612112) | | |
| ID: 130062247 | ATAC-STARR-seq lymphoblastoid active region 13135 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (21604968..21605037) | | |
| ID: 130062246 | ATAC-STARR-seq lymphoblastoid active region 13134 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (21602254..21602333) | | |
| ID: 130062245 | ATAC-STARR-seq lymphoblastoid active region 13133 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (21600410..21600929) | | |
| ID: 127888923 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr18:19173073-19173800 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (21593112..21593839) | | |
| ID: 127888922 | NANOG-H3K27ac hESC enhancer GRCh37_chr18:19171613-19172342 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (21591652..21592381) | | |
| ID: 127888921 | H3K27ac hESC enhancer GRCh37_chr18:18982491-18982990 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (21402530..21403029) | | |
| ID: 127888920 | H3K27ac hESC enhancer GRCh37_chr18:18981989-18982490 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (21402028..21402529) | | |
| ID: 127888919 | NANOG hESC enhancer GRCh37_chr18:18970956-18971808 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (21390995..21391847) | | |
| ID: 127888918 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr18:18966717-18967517 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (21386756..21387556) | | |
| ID: 127888917 | OCT4-NANOG hESC enhancer GRCh37_chr18:18922270-18922868 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (21342309..21342907) | | |
| ID: 127888916 | OCT4-NANOG hESC enhancer GRCh37_chr18:18842887-18843414 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (21262926..21263453) | | |
| ID: 124900410 | small nucleolar RNA SNORD23 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (21450653..21450756, complement) | | |
| ID: 121852959 | Sharpr-MPRA regulatory region 3945 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (21599048..21599342) | | |
| ID: 107985161 | uncharacterized LOC107985161 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (21140573..21180333, complement) | | |
| ID: 101927521 | uncharacterized LOC101927521 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (21380044..21451047, complement) | | |
| ID: 101927496 | GREB1L divergent transcript [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (21240675..21242728, complement) | | |
| ID: 100128324 | EXOG pseudogene 1 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (21180843..21183515, complement) | | |
| ID: 114799 | establishment of sister chromatid cohesion N-acetyltransferase 1 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (21529284..21600704, complement) | A930014I12Rik, CTF, ECO1, EFO1, ESO1 | 609674 |