ID: 132090372 | Neanderthal introgressed variant-containing enhancer experimental_43111 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (21527858..21528027) | | |
ID: 132090371 | Neanderthal introgressed variant-containing enhancer experimental_43023 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (21509134..21509303) | | |
ID: 130058624 | ATAC-STARR-seq lymphoblastoid silent region 7257 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (21599564..21600183) | | |
ID: 130058623 | ATAC-STARR-seq lymphoblastoid active region 10557 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (21541823..21541872) | | |
ID: 130058622 | ATAC-STARR-seq lymphoblastoid active region 10556 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (21514024..21514113) | | |
ID: 129663779 | ReSE screen-validated silencer GRCh37_chr16:21529065-21529231 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (21517744..21517910) | | |
ID: 127883435 | H3K27ac hESC enhancer GRCh37_chr16:22593503-22594003 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (22582182..22582682) | | |
ID: 127883417 | H3K27ac hESC enhancer GRCh37_chr16:21611613-21612177 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (21600292..21600856) | | |
ID: 127883416 | H3K4me1 hESC enhancer GRCh37_chr16:21565604-21566414 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (21554283..21555093) | | |
ID: 127883415 | H3K4me1 hESC enhancer GRCh37_chr16:21562361-21562862 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (21551040..21551541) | | |
ID: 127883414 | H3K4me1 hESC enhancer GRCh37_chr16:21561118-21561618 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (21549797..21550297) | | |
ID: 127883413 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:21552333-21553071 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (21541012..21541750) | | |
ID: 127883412 | H3K4me1 hESC enhancer GRCh37_chr16:21549827-21550326 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (21538506..21539005) | | |
ID: 127883411 | H3K4me1 hESC enhancer GRCh37_chr16:21549325-21549826 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (21538004..21538505) | | |
ID: 127883410 | H3K4me1 hESC enhancer GRCh37_chr16:21538112-21538922 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (21526791..21527601) | | |
ID: 127883409 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:21537301-21538111 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (21525980..21526790) | | |
ID: 127883408 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:21536490-21537300 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (21525169..21525979) | | |
ID: 127883407 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:21535062-21535794 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (21523741..21524473) | | |
ID: 127883406 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:21532860-21533594 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (21521539..21522273) | | |
ID: 127883405 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:21532127-21532859 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (21520806..21521538) | | |