| ID: 132090898 | Neanderthal introgressed variant-containing enhancer experimental_47746 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (11657751..11657920) | | |
| ID: 130062186 | ATAC-STARR-seq lymphoblastoid active region 13096 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (11851774..11851823) | | |
| ID: 130062185 | ATAC-STARR-seq lymphoblastoid active region 13095 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (11851266..11851505) | | |
| ID: 129664208 | ReSE screen-validated silencer GRCh37_chr18:11796263-11796399 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (11796264..11796400) | | |
| ID: 127888811 | H3K27ac hESC enhancer GRCh37_chr18:11775153-11775652 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (11775154..11775653) | | |
| ID: 127888810 | H3K4me1 hESC enhancer GRCh37_chr18:11737507-11738276 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (11737508..11738277) | | |
| ID: 127888809 | H3K4me1 hESC enhancer GRCh37_chr18:11732672-11733280 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (11732673..11733281) | | |
| ID: 127888808 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr18:11714059-11714618 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (11714060..11714619) | | |
| ID: 127888807 | H3K4me1 hESC enhancer GRCh37_chr18:11696745-11697246 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (11696746..11697247) | | |
| ID: 127888806 | H3K27ac hESC enhancer GRCh37_chr18:11689154-11689654 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (11689067..11689655) | | |
| ID: 126862697 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr18:11856862-11858061 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (11856863..11858062) | | |
| ID: 125368547 | Sharpr-MPRA regulatory region 95 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (11851830..11852124) | | |
| ID: 124904251 | uncharacterized LOC124904251 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (11857161..11860511, complement) | | |
| ID: 102465690 | microRNA 7153 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (11654885..11654941, complement) | hsa-mir-7153, mir-7153 | |
| ID: 100423060 | ASNS pseudogene 6 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (11746650..11747707) | | |
| ID: 57132 | charged multivesicular body protein 1B [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (11851413..11854444) | C10orf2, C18-ORF2, C18orf2, CHMP1.5, Vps46-2, Vps46B, hVps46-2 | 606486 |
| ID: 2774 | G protein subunit alpha L [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (11689264..11885685) | DYT25, HG1O | 139312 |