ID: 132090900 | Neanderthal introgressed variant-containing enhancer experimental_50263 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (74269107..74269276) | | |
ID: 132090526 | Neanderthal introgressed variant-containing enhancer experimental_50341 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (74316047..74316216) | | |
ID: 132090525 | Neanderthal introgressed variant-containing enhancer experimental_50334 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (74310864..74311033) | | |
ID: 132090524 | Neanderthal introgressed variant-containing enhancer experimental_50330 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (74309819..74309988) | | |
ID: 132090523 | Neanderthal introgressed variant-containing enhancer experimental_50307 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (74292882..74293051) | | |
ID: 132090522 | Neanderthal introgressed variant-containing enhancer experimental_50303 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (74292004..74292173) | | |
ID: 132090521 | Neanderthal introgressed variant-containing enhancer experimental_50301 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (74291755..74291924) | | |
ID: 132090520 | Neanderthal introgressed variant-containing enhancer experimental_50293 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (74285885..74286054) | | |
ID: 132090519 | Neanderthal introgressed variant-containing enhancer experimental_50279 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (74275984..74276153) | | |
ID: 130062714 | ATAC-STARR-seq lymphoblastoid active region 13495 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (74292463..74292522) | | |
ID: 129391005 | MPRA-validated peak3184 silencer [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (74300481..74300681) | | |
ID: 127889544 | H3K4me1 hESC enhancer GRCh37_chr18:71957777-71958384 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (74290542..74291149) | | |
ID: 127889543 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr18:71948314-71948841 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (74281079..74281606) | | |
ID: 127889542 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr18:71935092-71935632 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (74267857..74268397) | | |
ID: 127889541 | NANOG-H3K27ac hESC enhancer GRCh37_chr18:71917515-71918450 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (74250280..74251215) | | |
ID: 127889540 | H3K4me1 hESC enhancer GRCh37_chr18:71904867-71905366 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (74237632..74238131) | | |
ID: 121627839 | Sharpr-MPRA regulatory region 12176 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (74242614..74242908) | | |
ID: 106479422 | RNA, 7SL, cytoplasmic 551, pseudogene [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (74227506..74227802) | | |
ID: 644041 | chromosome 18 open reading frame 63 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (74315839..74359189) | DKFZP781G0119 | |
ID: 1528 | cytochrome b5 type A [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (74250846..74291963, complement) | CYB5, MCB5, METAG | 613218 |