ID: 132090516 | Neanderthal introgressed variant-containing enhancer experimental_50021 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (73528737..73528906) | | |
ID: 132090515 | Neanderthal introgressed variant-containing enhancer experimental_49987 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (73450579..73450748) | | |
ID: 132090514 | Neanderthal introgressed variant-containing enhancer experimental_49980 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (73425318..73425487) | | |
ID: 132090513 | Neanderthal introgressed variant-containing enhancer experimental_49950 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (73342517..73342686) | | |
ID: 129664271 | ReSE screen-validated silencer GRCh37_chr18:70926050-70926267 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (73258815..73259032) | | |
ID: 127889538 | H3K27ac hESC enhancer GRCh37_chr18:71359027-71359527 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (73691792..73692292) | | |
ID: 127889537 | H3K27ac hESC enhancer GRCh37_chr18:71358526-71359026 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (73691291..73691791) | | |
ID: 127889536 | OCT4-NANOG hESC enhancer GRCh37_chr18:71098754-71099424 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (73431519..73432189) | | |
ID: 127889535 | H3K4me1 hESC enhancer GRCh37_chr18:70931223-70931724 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (73263988..73264489) | | |
ID: 127889534 | OCT4-NANOG hESC enhancer GRCh37_chr18:70912438-70913029 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (73245203..73245794) | | |
ID: 126862795 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr18:71384186-71385385 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (73716951..73718150) | | |
ID: 126862794 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr18:71382077-71383276 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (73714842..73716041) | | |
ID: 126862793 | MED14-independent group 3 enhancer GRCh37_chr18:71362654-71363853 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (73695419..73696618) | | |
ID: 126862792 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr18:71230790-71231989 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (73563555..73564754) | | |
ID: 126862791 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr18:70916635-70917834 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (73249400..73250599) | | |
ID: 121627836 | Sharpr-MPRA regulatory region 3365 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (73189774..73190068) | | |
ID: 107992389 | chr18 t(4;18)(q35;q18) HERV-H recombination region [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (73325048..73328058) | | |
ID: 106480507 | RNA, 7SL, cytoplasmic 401, pseudogene [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (73744935..73745232) | | |
ID: 105372191 | uncharacterized LOC105372191 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (73756507..73784778) | | |
ID: 105372190 | uncharacterized LOC105372190 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (73378367..73691291, complement) | | |