ID: 132090439 | Neanderthal introgressed variant-containing enhancer experimental_46362 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (86382776..86382945) | | |
ID: 132090438 | Neanderthal introgressed variant-containing enhancer experimental_46360 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (86368172..86368341) | | |
ID: 129663916 | ReSE screen-validated silencer GRCh37_chr16:86466900-86467129 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (86433294..86433523) | | |
ID: 127884942 | H3K4me1 hESC enhancer GRCh37_chr16:86534107-86534663 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (86500501..86501057) | | |
ID: 127884941 | H3K4me1 hESC enhancer GRCh37_chr16:86531905-86532529 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (86498299..86498923) | | |
ID: 127884940 | H3K4me1 hESC enhancer GRCh37_chr16:86410784-86411320 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (86377178..86377714) | | |
ID: 127884939 | H3K4me1 hESC enhancer GRCh37_chr16:86393693-86394193 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (86360087..86360587) | | |
ID: 127884938 | H3K4me1 hESC enhancer GRCh37_chr16:86342206-86342723 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (86308600..86309117) | | |
ID: 127884937 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:86331997-86332570 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (86298391..86298964) | | |
ID: 127884936 | H3K4me1 hESC enhancer GRCh37_chr16:86329547-86330048 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (86295941..86296442) | | |
ID: 126862433 | BRD4-independent group 4 enhancer GRCh37_chr16:86499943-86501142 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (86466337..86467536) | | |
ID: 126862432 | BRD4-independent group 4 enhancer GRCh37_chr16:86340947-86342146 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (86307341..86308540) | | |
ID: 125177386 | Sharpr-MPRA regulatory region 8769 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (86337223..86338273) | | |
ID: 125177385 | Sharpr-MPRA regulatory region 7763 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (86301023..86301720) | | |
ID: 124903745 | uncharacterized LOC124903745 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (86317549..86318535, complement) | | |
ID: 121847998 | Sharpr-MPRA regulatory region 1422 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (86424590..86425197) | | |
ID: 108281164 | LINC00917-FENDRR intergenic CAGE-defined mid-level expression enhancer [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (86383803..86384362) | | |
ID: 105943583 | VISTA enhancer hs1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (86396481..86397524) | | |
ID: 732275 | long intergenic non-protein coding RNA 917 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (86331850..86345679, complement) | | |
ID: 401864 | chloride intracellular channel 1 pseudogene [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (86434844..86435498, complement) | | |